Linked Data
dbSNP Id:
rs759561106
gnomAD v3:
2-31533615-G-T
gnomAD v4:
2-31533615-G-T
MyVariant Identifiers:
chr2:g.31758685G>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.31533615G>T , CM000664.2:g.31533615G>T | GRCh38 |
| NC_000002.11:g.31758685G>T , CM000664.1:g.31758685G>T | GRCh37 |
| NC_000002.10:g.31612189G>T | NCBI36 |
| NG_008365.1:g.52357C>A |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000622030.2:c.433C>A MANE Select | ENSP00000477587.1:p.Arg145= | |
| ENST00000622030.1:c.433C>A | ENSP00000477587.1:p.Arg145= | |
| NM_000348.3:c.433C>A | NP_000339.2:p.Arg145= | |
| XM_011533068.1:c.433C>A | XP_011531370.1:p.Arg145= | |
| XM_011533069.1:c.211C>A | XP_011531371.1:p.Arg71= | |
| XM_011533070.1:c.178C>A | XP_011531372.1:p.Arg60= | |
| XM_011533071.1:c.178C>A | XP_011531373.1:p.Arg60= | |
| XM_011533072.1:c.178C>A | XP_011531374.1:p.Arg60= | |
| XM_011533069.2:c.211C>A | XP_011531371.1:p.Arg71= | |
| XM_011533072.2:c.178C>A | XP_011531374.1:p.Arg60= | |
| NM_000348.4:c.433C>A MANE Select | NP_000339.2:p.Arg145= |