Linked Data
dbSNP Id:
rs371616363
ExAC:
7:44187428 C / T
gnomAD v2:
7-44187428-C-T
gnomAD v3:
7-44147829-C-T
gnomAD v4:
7-44147829-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.44147829C>T , CM000669.2:g.44147829C>T | GRCh38 |
| NC_000007.13:g.44187428C>T , CM000669.1:g.44187428C>T | GRCh37 |
| NC_000007.12:g.44153953C>T | NCBI36 |
| NG_008847.1:g.46595G>A | |
| NG_008847.2:g.55342G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000395796.8:c.*682G>A | ENSP00000379142.4:n.*682G>A | |
| ENST00000616242.5:c.684G>A | ENSP00000482149.2:p.Thr228= | |
| ENST00000345378.7:c.687G>A | ENSP00000223366.2:p.Thr229= | |
| ENST00000403799.8:c.684G>A MANE Select | ENSP00000384247.3:p.Thr228= | |
| ENST00000671824.1:c.684G>A | ENSP00000500264.1:p.Thr228= | |
| ENST00000673284.1:c.684G>A | ENSP00000499852.1:p.Thr228= | |
| ENST00000345378.6:c.687G>A | ENSP00000223366.2:p.Thr229= | |
| ENST00000395796.7:c.681G>A | ENSP00000379142.3:p.Thr227= | |
| ENST00000403799.7:c.684G>A | ENSP00000384247.3:p.Thr228= | |
| ENST00000437084.1:c.633G>A | ENSP00000402840.1:p.Thr211= | |
| ENST00000616242.4:c.681G>A | ENSP00000482149.1:p.Thr227= | |
| NM_000162.3:c.684G>A | NP_000153.1:p.Thr228= | |
| NM_033507.1:c.687G>A | NP_277042.1:p.Thr229= | |
| NM_033508.1:c.681G>A | NP_277043.1:p.Thr227= | |
| XR_927223.1:n.82+81C>T | ||
| NM_000162.4:c.684G>A | NP_000153.1:p.Thr228= | |
| NM_001354800.1:c.684G>A | NP_001341729.1:p.Thr228= | |
| NM_033507.2:c.687G>A | NP_277042.1:p.Thr229= | |
| NM_033508.2:c.681G>A | NP_277043.1:p.Thr227= | |
| XR_927223.2:n.82+81C>T | ||
| NM_000162.5:c.684G>A MANE Select | NP_000153.1:p.Thr228= | |
| NM_033507.3:c.687G>A | NP_277042.1:p.Thr229= | |
| NM_033508.3:c.681G>A | NP_277043.1:p.Thr227= |