Canonical Allele Identifier: CA1427019584
Gene: AHSG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.186620644T= , CM000665.2:g.186620644T= GRCh38
NC_000003.11:g.186338433T= , CM000665.1:g.186338433T= GRCh37
NC_000003.10:g.187821127T= NCBI36
NG_011436.1:g.12584T=

Transcript Alleles

HGVS Amino-acid change
ENST00000411641.7:c.818T= MANE Select ENSP00000393887.2:p.Val273=
ENST00000273784.5:c.821T= ENSP00000273784.5:p.Val274=
ENST00000411641.6:c.818T= ENSP00000393887.2:p.Val273=
NM_001622.2:c.818T= NP_001613.2:p.Val273=
NM_001354571.1:c.821T= NP_001341500.1:p.Val274=
NM_001354572.1:c.815T= NP_001341501.1:p.Val272=
NM_001354573.1:c.734T= NP_001341502.1:p.Val245=
NM_001622.3:c.818T= NP_001613.2:p.Val273=
NM_001622.4:c.818T= MANE Select NP_001613.2:p.Val273=
NM_001354571.2:c.821T= NP_001341500.1:p.Val274=
NM_001354572.2:c.815T= NP_001341501.1:p.Val272=
NM_001354573.2:c.734T= NP_001341502.1:p.Val245=