Linked Data
dbSNP Id:
rs559792321
gnomAD v2:
12-103238038-C-T
gnomAD v3:
12-102844260-C-T
gnomAD v4:
12-102844260-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.102844260C>T , CM000674.2:g.102844260C>T | GRCh38 |
| NC_000012.11:g.103238038C>T , CM000674.1:g.103238038C>T | GRCh37 |
| NC_000012.10:g.101762168C>T | NCBI36 |
| NG_008690.1:g.78343G>A | |
| NG_008690.2:g.119151G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000553106.6:c.1065+76G>A MANE Select | ENSP00000448059.1:n.1065+76G>A | |
| ENST00000307000.7:c.1050+76G>A | ENSP00000303500.2:n.1050+76G>A | |
| ENST00000549247.6:n.824+76G>A | ||
| ENST00000551114.2:n.727+76G>A | ||
| ENST00000553106.5:c.1065+76G>A | ENSP00000448059.1:n.1065+76G>A | |
| ENST00000635477.1:c.169+76G>A | ||
| ENST00000635528.1:n.580+76G>A | ||
| NM_000277.1:c.1065+76G>A | NP_000268.1:n.1065+76G>A | |
| XM_011538422.1:c.1008+76G>A | XP_011536724.1:n.1008+76G>A | |
| NM_000277.2:c.1065+76G>A | NP_000268.1:n.1065+76G>A | |
| NM_001354304.1:c.1065+76G>A | NP_001341233.1:n.1065+76G>A | |
| NM_000277.3:c.1065+76G>A MANE Select | NP_000268.1:n.1065+76G>A | |
| NM_001354304.2:c.1065+76G>A | NP_001341233.1:n.1065+76G>A |