HGVS | Genome Assembly |
---|---|
NC_000001.11:g.15930526A= , CM000663.2:g.15930526A= | GRCh38 |
NC_000001.10:g.16257021A= , CM000663.1:g.16257021A= | GRCh37 |
NC_000001.9:g.16129608A= | NCBI36 |
NG_050663.1:g.87663A= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000438066.2:c.*5137A= | ENSP00000388021.2:n.*5137A= | |
ENST00000375759.8:c.4286A= MANE Select | ENSP00000364912.3:p.Asn1429= | |
ENST00000375759.7:c.4286A= | ENSP00000364912.3:p.Asn1429= | |
NM_015001.2:c.4286A= | NP_055816.2:p.Asn1429= | |
NM_015001.3:c.4286A= MANE Select | NP_055816.2:p.Asn1429= |