Linked Data
dbSNP Id:
rs1656900931
gnomAD v4:
1-203225680-G-A
MyVariant Identifiers:
chr1:g.203194808G>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.203225680G>A , CM000663.2:g.203225680G>A | GRCh38 |
| NC_000001.10:g.203194808G>A , CM000663.1:g.203194808G>A | GRCh37 |
| NC_000001.9:g.201461431G>A | NCBI36 |
| NG_012867.1:g.9053C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000367229.6:c.246C>T MANE Select | ENSP00000356198.1:p.Gly82= | |
| ENST00000255427.7:c.246C>T | ENSP00000255427.3:p.Gly82= | |
| ENST00000367229.5:c.246C>T | ENSP00000356198.1:p.Gly82= | |
| ENST00000484834.5:n.4603C>T | ||
| ENST00000491855.5:c.246C>T | ENSP00000423778.1:p.Gly82= | |
| ENST00000503786.1:c.246C>T | ENSP00000421617.1:p.Gly82= | |
| ENST00000513472.5:n.442C>T | ||
| NM_001256125.1:c.246C>T | NP_001243054.2:p.Gly82= | |
| NM_001270509.1:c.246C>T | NP_001257438.1:p.Gly82= | |
| NM_003465.2:c.246C>T | NP_003456.1:p.Gly82= | |
| NR_045784.1:n.342C>T | ||
| NR_045785.1:n.342C>T | ||
| XM_011509109.1:c.291C>T | XP_011507411.1:p.Gly97= | |
| XM_011509110.1:c.291C>T | XP_011507412.1:p.Gly97= | |
| XR_921732.1:n.291C>T | ||
| NM_003465.3:c.246C>T MANE Select | NP_003456.1:p.Gly82= | |
| NM_001256125.2:c.246C>T | NP_001243054.2:p.Gly82= | |
| NR_045784.2:n.283C>T | ||
| NR_045785.2:n.283C>T |