Linked Data
dbSNP Id:
rs772916866
gnomAD v2:
X-8700147-G-T
gnomAD v3:
X-8732106-G-T
gnomAD v4:
X-8732106-G-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.8732106G>T , CM000685.2:g.8732106G>T | GRCh38 |
| NC_000023.10:g.8700147G>T , CM000685.1:g.8700147G>T | GRCh37 |
| NC_000023.9:g.8660147G>T | NCBI36 |
| NG_007088.1:g.5081C>A | |
| NG_007088.2:g.5081C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000262648.8:c.-70C>A MANE Select | ENSP00000262648.3:n.-70C>A | |
| ENST00000262648.7:c.-70C>A | ENSP00000262648.3:n.-70C>A | |
| ENST00000619786.1:c.-70C>A | ENSP00000478734.1:n.-70C>A | |
| NM_000216.2:c.-70C>A | NP_000207.2:n.-70C>A | |
| XM_005274501.3:c.-70C>A | XP_005274558.1:n.-70C>A | |
| NM_000216.3:c.-70C>A | NP_000207.2:n.-70C>A | |
| XM_005274501.4:c.-70C>A | XP_005274558.1:n.-70C>A | |
| NM_000216.4:c.-70C>A MANE Select | NP_000207.2:n.-70C>A |