Linked Data
ClinVar Variation Id:
352656
ClinVar RCV Id:
RCV000284562
dbSNP Id:
rs424740
gnomAD v2:
5-161581035-T-A
gnomAD v3:
5-162154029-T-A
gnomAD v4:
5-162154029-T-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.162154029T>A , CM000667.2:g.162154029T>A | GRCh38 |
| NC_000005.9:g.161581035T>A , CM000667.1:g.161581035T>A | GRCh37 |
| NC_000005.8:g.161513613T>A | NCBI36 |
| NG_009290.1:g.91388T>A |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000356592.8:c.2090T>A | ||
| ENST00000361925.9:c.*661T>A | ENSP00000354651.5:n.*661T>A | |
| ENST00000638552.1:c.*661T>A | ENSP00000491763.1:n.*661T>A | |
| ENST00000638660.1:c.*661T>A | ENSP00000492869.1:n.*661T>A | |
| ENST00000638772.1:c.*4686T>A | ENSP00000491557.1:n.*4686T>A | |
| ENST00000638877.1:c.1966T>A | ||
| ENST00000639046.1:c.*661T>A | ENSP00000492659.1:n.*661T>A | |
| ENST00000639111.2:c.*661T>A | ENSP00000492125.2:n.*661T>A | |
| ENST00000639213.2:c.*661T>A MANE Select | ENSP00000491909.2:n.*661T>A | |
| ENST00000639278.1:c.2752T>A | ENSP00000491958.1:n.2752T>A | |
| ENST00000639384.1:c.*2270T>A | ENSP00000491240.1:n.*2270T>A | |
| ENST00000639424.1:c.*1289T>A | ENSP00000491245.1:n.*1289T>A | |
| ENST00000639683.1:c.*661T>A | ENSP00000492581.1:n.*661T>A | |
| ENST00000639975.1:c.*661T>A | ENSP00000492096.1:n.*661T>A | |
| ENST00000640500.1:n.1363T>A | ||
| ENST00000640739.1:n.7036T>A | ||
| ENST00000640985.1:c.*661T>A | ENSP00000492293.1:n.*661T>A | |
| ENST00000641017.1:c.2158T>A | ENSP00000493461.1:n.2158T>A | |
| ENST00000356592.7:c.*661T>A | ENSP00000349000.3:n.*661T>A | |
| ENST00000414552.6:c.*661T>A | ENSP00000410732.2:n.*661T>A | |
| ENST00000522990.5:c.*1667T>A | ENSP00000430732.1:n.*1667T>A | |
| NM_000816.3:c.*661T>A | NP_000807.2:n.*661T>A | |
| NM_198903.2:c.*661T>A | NP_944493.2:n.*661T>A | |
| NM_198904.2:c.*661T>A | NP_944494.1:n.*661T>A | |
| NM_001375339.1:c.*661T>A | NP_001362268.1:n.*661T>A | |
| NM_001375340.1:c.*923T>A | NP_001362269.1:n.*923T>A | |
| NM_001375341.1:c.*661T>A | NP_001362270.1:n.*661T>A | |
| NM_001375342.1:c.*661T>A | NP_001362271.1:n.*661T>A | |
| NM_001375343.1:c.*661T>A | NP_001362272.1:n.*661T>A | |
| NM_001375344.1:c.*661T>A | NP_001362273.1:n.*661T>A | |
| NM_001375345.1:c.*661T>A | NP_001362274.1:n.*661T>A | |
| NM_001375346.1:c.*661T>A | NP_001362275.1:n.*661T>A | |
| NM_001375347.1:c.*661T>A | NP_001362276.1:n.*661T>A | |
| NM_001375348.1:c.*661T>A | NP_001362277.1:n.*661T>A | |
| NM_001375349.1:c.*661T>A | NP_001362278.1:n.*661T>A | |
| NM_001375350.1:c.*661T>A | NP_001362279.1:n.*661T>A | |
| NM_198904.3:c.*661T>A | NP_944494.1:n.*661T>A | |
| NM_198904.4:c.*661T>A MANE Select | NP_944494.1:n.*661T>A |