HGVS | Genome Assembly |
---|---|
NC_000015.10:g.73323132G>C , CM000677.2:g.73323132G>C | GRCh38 |
NC_000015.9:g.73615473G>C , CM000677.1:g.73615473G>C | GRCh37 |
NC_000015.8:g.71402526G>C | NCBI36 |
NG_009063.1:g.51133C>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000261917.4:c.2961C>G MANE Select | ENSP00000261917.3:p.Ala987= | |
ENST00000261917.3:c.2961C>G | ENSP00000261917.3:p.Ala987= | |
NM_005477.2:c.2961C>G | NP_005468.1:p.Ala987= | |
XM_011521148.1:c.1743C>G | XP_011519450.1:p.Ala581= | |
XM_011521148.2:c.1743C>G | XP_011519450.1:p.Ala581= | |
NM_005477.3:c.2961C>G MANE Select | NP_005468.1:p.Ala987= |