Linked Data
ClinVar Variation Id:
3068513
ClinVar RCV Id:
RCV003993705
dbSNP Id:
rs1441779135
gnomAD v2:
7-44191869-C-T
gnomAD v4:
7-44152270-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.44152270C>T , CM000669.2:g.44152270C>T | GRCh38 |
| NC_000007.13:g.44191869C>T , CM000669.1:g.44191869C>T | GRCh37 |
| NC_000007.12:g.44158394C>T | NCBI36 |
| NG_008847.1:g.42154G>A | |
| NG_008847.2:g.50901G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000395796.8:c.*361+1G>A | ENSP00000379142.4:n.*361+1G>A | |
| ENST00000616242.5:c.363+1G>A | ENSP00000482149.2:n.363+1G>A | |
| ENST00000682635.1:n.849+1G>A | ||
| ENST00000345378.7:c.366+1G>A | ENSP00000223366.2:n.366+1G>A | |
| ENST00000403799.8:c.363+1G>A MANE Select | ENSP00000384247.3:n.363+1G>A | |
| ENST00000671824.1:c.363+1G>A | ENSP00000500264.1:n.363+1G>A | |
| ENST00000673284.1:c.363+1G>A | ENSP00000499852.1:n.363+1G>A | |
| ENST00000345378.6:c.366+1G>A | ENSP00000223366.2:n.366+1G>A | |
| ENST00000395796.7:c.360+1G>A | ENSP00000379142.3:n.360+1G>A | |
| ENST00000403799.7:c.363+1G>A | ENSP00000384247.3:n.363+1G>A | |
| ENST00000437084.1:c.363+1G>A | ENSP00000402840.1:n.363+1G>A | |
| ENST00000616242.4:c.360+1G>A | ENSP00000482149.1:n.360+1G>A | |
| NM_000162.3:c.363+1G>A | NP_000153.1:n.363+1G>A | |
| NM_033507.1:c.366+1G>A | NP_277042.1:n.366+1G>A | |
| NM_033508.1:c.360+1G>A | NP_277043.1:n.360+1G>A | |
| NM_000162.4:c.363+1G>A | NP_000153.1:n.363+1G>A | |
| NM_001354800.1:c.363+1G>A | NP_001341729.1:n.363+1G>A | |
| NM_033507.2:c.366+1G>A | NP_277042.1:n.366+1G>A | |
| NM_033508.2:c.360+1G>A | NP_277043.1:n.360+1G>A | |
| NM_000162.5:c.363+1G>A MANE Select | NP_000153.1:n.363+1G>A | |
| NM_033507.3:c.366+1G>A | NP_277042.1:n.366+1G>A | |
| NM_033508.3:c.360+1G>A | NP_277043.1:n.360+1G>A |