HGVS | Genome Assembly |
---|---|
NC_000015.10:g.73329661A>G , CM000677.2:g.73329661A>G | GRCh38 |
NC_000015.9:g.73622002A>G , CM000677.1:g.73622002A>G | GRCh37 |
NC_000015.8:g.71409055A>G | NCBI36 |
NG_009063.1:g.44604T>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000261917.4:c.1502T>C MANE Select | ENSP00000261917.3:p.Val501Ala | |
ENST00000261917.3:c.1502T>C | ENSP00000261917.3:p.Val501Ala | |
NM_005477.2:c.1502T>C | NP_005468.1:p.Val501Ala | |
XM_011521148.1:c.284T>C | XP_011519450.1:p.Val95Ala | |
XM_011521148.2:c.284T>C | XP_011519450.1:p.Val95Ala | |
NM_005477.3:c.1502T>C MANE Select | NP_005468.1:p.Val501Ala |