MyVariant.info:
GRCh38
chr2:g.31580823G>A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.31580823G>A , CM000664.2:g.31580823G>A | GRCh38 |
| NG_008365.1:g.5149C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000622030.2:c.78C>T MANE Select | ENSP00000477587.1:p.Tyr26= | |
| ENST00000622030.1:c.78C>T | ENSP00000477587.1:p.Tyr26= | |
| NM_000348.3:c.78C>T | NP_000339.2:p.Tyr26= | |
| XM_011533068.1:c.78C>T | XP_011531370.1:p.Tyr26= | |
| XM_011533070.1:c.27-47057C>T | XP_011531372.1:n.27-47057C>T | |
| XM_011533071.1:c.27-47057C>T | XP_011531373.1:n.27-47057C>T | |
| XM_011533072.1:c.27-47057C>T | XP_011531374.1:n.27-47057C>T | |
| XM_011533072.2:c.27-47057C>T | XP_011531374.1:n.27-47057C>T | |
| NM_000348.4:c.78C>T MANE Select | NP_000339.2:p.Tyr26= |