Linked Data
dbSNP Id:
rs746106548
ExAC:
12:103310953 G / A
gnomAD v2:
12-103310953-G-A
gnomAD v3:
12-102917175-G-A
gnomAD v4:
12-102917175-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.102917175G>A , CM000674.2:g.102917175G>A | GRCh38 |
| NC_000012.11:g.103310953G>A , CM000674.1:g.103310953G>A | GRCh37 |
| NC_000012.10:g.101835083G>A | NCBI36 |
| NG_008690.1:g.5428C>T | |
| NG_008690.2:g.46236C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000553106.6:c.-45C>T MANE Select | ENSP00000448059.1:n.-45C>T | |
| ENST00000307000.7:c.-192C>T | ENSP00000303500.2:n.-192C>T | |
| ENST00000546708.5:n.543C>T | ||
| ENST00000546844.1:c.-45C>T | ENSP00000446658.1:n.-45C>T | |
| ENST00000547319.1:n.267C>T | ||
| ENST00000549111.5:n.52C>T | ||
| ENST00000551337.5:c.-45C>T | ENSP00000447620.1:n.-45C>T | |
| ENST00000551988.5:n.45C>T | ||
| ENST00000553106.5:c.-45C>T | ENSP00000448059.1:n.-45C>T | |
| ENST00000635500.1:n.29-4277C>T | ||
| NM_000277.1:c.-45C>T | NP_000268.1:n.-45C>T | |
| XM_011538422.1:c.-45C>T | XP_011536724.1:n.-45C>T | |
| NM_000277.2:c.-45C>T | NP_000268.1:n.-45C>T | |
| NM_001354304.1:c.-45C>T | NP_001341233.1:n.-45C>T | |
| XM_017019370.2:c.-45C>T | XP_016874859.1:n.-45C>T | |
| NM_000277.3:c.-45C>T MANE Select | NP_000268.1:n.-45C>T | |
| NM_001354304.2:c.-45C>T | NP_001341233.1:n.-45C>T |