HGVS | Genome Assembly |
---|---|
NC_000015.10:g.73322999G= , CM000677.2:g.73322999G= | GRCh38 |
NC_000015.9:g.73615340G= , CM000677.1:g.73615340G= | GRCh37 |
NC_000015.8:g.71402393G= | NCBI36 |
NG_009063.1:g.51266C= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000261917.4:c.3094C= MANE Select | ENSP00000261917.3:p.Pro1032= | |
ENST00000261917.3:c.3094C= | ENSP00000261917.3:p.Pro1032= | |
NM_005477.2:c.3094C= | NP_005468.1:p.Pro1032= | |
XM_011521148.1:c.1876C= | XP_011519450.1:p.Pro626= | |
XM_011521148.2:c.1876C= | XP_011519450.1:p.Pro626= | |
NM_005477.3:c.3094C= MANE Select | NP_005468.1:p.Pro1032= |