Linked Data
MyVariant Identifiers:
chr2:g.31805725T>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.31580655T>C , CM000664.2:g.31580655T>C | GRCh38 |
| NC_000002.11:g.31805725T>C , CM000664.1:g.31805725T>C | GRCh37 |
| NC_000002.10:g.31659229T>C | NCBI36 |
| NG_008365.1:g.5317A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000622030.2:c.246A>G MANE Select | ENSP00000477587.1:p.Val82= | |
| ENST00000622030.1:c.246A>G | ENSP00000477587.1:p.Val82= | |
| NM_000348.3:c.246A>G | NP_000339.2:p.Val82= | |
| XM_011533068.1:c.246A>G | XP_011531370.1:p.Val82= | |
| XM_011533070.1:c.27-46889A>G | XP_011531372.1:n.27-46889A>G | |
| XM_011533071.1:c.27-46889A>G | XP_011531373.1:n.27-46889A>G | |
| XM_011533072.1:c.27-46889A>G | XP_011531374.1:n.27-46889A>G | |
| XM_011533072.2:c.27-46889A>G | XP_011531374.1:n.27-46889A>G | |
| NM_000348.4:c.246A>G MANE Select | NP_000339.2:p.Val82= |