Linked Data
ClinVar Variation Id:
359999
dbSNP Id:
rs886062271
gnomAD v3:
7-30594863-C-T
gnomAD v4:
7-30594863-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.30594863C>T , CM000669.2:g.30594863C>T | GRCh38 |
| NC_000007.13:g.30634479C>T , CM000669.1:g.30634479C>T | GRCh37 |
| NC_000007.12:g.30601004C>T | NCBI36 |
| NG_007942.1:g.5299C>T , LRG_243:g.5299C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000470392.2:n.32C>T | ||
| ENST00000478124.6:n.5C>T | ||
| ENST00000485784.2:n.21C>T | ||
| ENST00000674643.1:c.-59C>T | ENSP00000501636.1:n.-59C>T | |
| ENST00000674807.1:c.-59C>T | ENSP00000502814.1:n.-59C>T | |
| ENST00000674815.1:c.-237C>T | ENSP00000502799.1:n.-237C>T | |
| ENST00000675051.1:c.22-3933C>T | ENSP00000502296.1:n.22-3933C>T | |
| ENST00000675529.1:c.-59C>T | ENSP00000501655.1:n.-59C>T | |
| ENST00000675810.1:c.-59C>T | ENSP00000502743.1:n.-59C>T | |
| ENST00000676088.1:c.-59C>T | ENSP00000501884.1:n.-59C>T | |
| ENST00000676210.1:c.-59C>T | ENSP00000502373.1:n.-59C>T | |
| ENST00000676403.1:c.-59C>T | ENSP00000502681.1:n.-59C>T | |
| ENST00000389266.7:c.-59C>T | ENSP00000373918.3:n.-59C>T | |
| ENST00000454308.5:c.-59C>T | ENSP00000392677.1:n.-59C>T | |
| ENST00000627489.1:c.-59C>T | ENSP00000485931.1:n.-59C>T | |
| NM_001316772.1:c.-221C>T | NP_001303701.1:n.-221C>T | |
| NM_002047.2:c.-59C>T , LRG_243t1:c.-59C>T | NP_002038.2:n.-59C>T | |
| XM_006715686.2:c.-538C>T | XP_006715749.1:n.-538C>T |