HGVS | Genome Assembly |
---|---|
NC_000006.12:g.49612406C= , CM000668.2:g.49612406C= | GRCh38 |
NC_000006.11:g.49580119C= , CM000668.1:g.49580119C= | GRCh37 |
NC_000006.10:g.49688078C= | NCBI36 |
NG_011704.1:g.29469G= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000371175.10:c.936G= MANE Select | ENSP00000360217.4:p.Lys312= | |
ENST00000646272.1:c.936G= | ENSP00000494337.1:p.Lys312= | |
ENST00000646939.1:c.936G= | ENSP00000494709.1:p.Lys312= | |
ENST00000646963.1:c.936G= | ENSP00000495337.1:p.Lys312= | |
ENST00000229810.9:c.936G= | ENSP00000229810.8:p.Lys312= | |
ENST00000371175.8:c.936G= | ENSP00000360217.4:p.Lys312= | |
ENST00000618248.3:c.936G= | ENSP00000482984.1:p.Lys312= | |
NM_000324.2:c.936G= | NP_000315.2:p.Lys312= | |
NM_000324.3:c.936G= MANE Select | NP_000315.2:p.Lys312= |