HGVS | Genome Assembly |
---|---|
NC_000015.10:g.73367786G= , CM000677.2:g.73367786G= | GRCh38 |
NC_000015.9:g.73660127G= , CM000677.1:g.73660127G= | GRCh37 |
NC_000015.8:g.71447180G= | NCBI36 |
NG_009063.1:g.6479C= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000261917.4:c.485C= MANE Select | ENSP00000261917.3:p.Ala162= | |
ENST00000261917.3:c.485C= | ENSP00000261917.3:p.Ala162= | |
NM_005477.2:c.485C= | NP_005468.1:p.Ala162= | |
NM_005477.3:c.485C= MANE Select | NP_005468.1:p.Ala162= |