Linked Data
ClinVar Variation Id:
2121221
ClinVar RCV Id:
RCV003049053
dbSNP Id:
rs761204125
ExAC:
7:44185148 C / T
gnomAD v2:
7-44185148-C-T
gnomAD v3:
7-44145549-C-T
gnomAD v4:
7-44145549-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.44145549C>T , CM000669.2:g.44145549C>T | GRCh38 |
| NC_000007.13:g.44185148C>T , CM000669.1:g.44185148C>T | GRCh37 |
| NC_000007.12:g.44151673C>T | NCBI36 |
| NG_008847.1:g.48875G>A | |
| NG_008847.2:g.57622G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000395796.8:c.*1199G>A | ENSP00000379142.4:n.*1199G>A | |
| ENST00000616242.5:c.*321G>A | ENSP00000482149.2:n.*321G>A | |
| ENST00000683378.1:n.427G>A | ||
| ENST00000336642.9:c.235G>A | ENSP00000338009.5:p.Val79Ile | |
| ENST00000345378.7:c.1204G>A | ENSP00000223366.2:p.Val402Ile | |
| ENST00000403799.8:c.1201G>A MANE Select | ENSP00000384247.3:p.Val401Ile | |
| ENST00000671824.1:c.1264G>A | ENSP00000500264.1:p.Val422Ile | |
| ENST00000672743.1:n.213G>A | ||
| ENST00000673284.1:c.1201G>A | ENSP00000499852.1:p.Val401Ile | |
| ENST00000336642.8:c.253G>A | ENSP00000338009.4:p.Val85Ile | |
| ENST00000345378.6:c.1204G>A | ENSP00000223366.2:p.Val402Ile | |
| ENST00000395796.7:c.1198G>A | ENSP00000379142.3:p.Val400Ile | |
| ENST00000403799.7:c.1201G>A | ENSP00000384247.3:p.Val401Ile | |
| ENST00000437084.1:c.1150G>A | ENSP00000402840.1:p.Val384Ile | |
| ENST00000459642.1:n.581G>A | ||
| ENST00000616242.4:c.1198G>A | ENSP00000482149.1:p.Val400Ile | |
| NM_000162.3:c.1201G>A | NP_000153.1:p.Val401Ile | |
| NM_033507.1:c.1204G>A | NP_277042.1:p.Val402Ile | |
| NM_033508.1:c.1198G>A | NP_277043.1:p.Val400Ile | |
| NM_000162.4:c.1201G>A | NP_000153.1:p.Val401Ile | |
| NM_001354800.1:c.1201G>A | NP_001341729.1:p.Val401Ile | |
| NM_001354801.1:c.190G>A | NP_001341730.1:p.Val64Ile | |
| NM_001354802.1:c.61G>A | NP_001341731.1:p.Val21Ile | |
| NM_001354803.1:c.235G>A | NP_001341732.1:p.Val79Ile | |
| NM_033507.2:c.1204G>A | NP_277042.1:p.Val402Ile | |
| NM_033508.2:c.1198G>A | NP_277043.1:p.Val400Ile | |
| XM_024446707.1:c.61G>A | XP_024302475.1:p.Val21Ile | |
| NM_000162.5:c.1201G>A MANE Select | NP_000153.1:p.Val401Ile | |
| NM_033507.3:c.1204G>A | NP_277042.1:p.Val402Ile | |
| NM_033508.3:c.1198G>A | NP_277043.1:p.Val400Ile | |
| NM_001354803.2:c.235G>A | NP_001341732.1:p.Val79Ile |