Canonical Allele Identifier: CA1427018712

Gene: AHSG

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.186618567C= , CM000665.2:g.186618567C=	GRCh38
NC_000003.11:g.186336356C= , CM000665.1:g.186336356C=	GRCh37
NC_000003.10:g.187819050C=	NCBI36
NG_011436.1:g.10507C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000411641.7:c.605C= MANE Select	ENSP00000393887.2:p.Thr202=
ENST00000273784.5:c.608C=	ENSP00000273784.5:p.Thr203=
ENST00000411641.6:c.605C=	ENSP00000393887.2:p.Thr202=
NM_001622.2:c.605C=	NP_001613.2:p.Thr202=
NM_001354571.1:c.608C=	NP_001341500.1:p.Thr203=
NM_001354572.1:c.602C=	NP_001341501.1:p.Thr201=
NM_001354573.1:c.605C=	NP_001341502.1:p.Thr202=
NM_001622.3:c.605C=	NP_001613.2:p.Thr202=
NM_001622.4:c.605C= MANE Select	NP_001613.2:p.Thr202=
NM_001354571.2:c.608C=	NP_001341500.1:p.Thr203=
NM_001354572.2:c.602C=	NP_001341501.1:p.Thr201=
NM_001354573.2:c.605C=	NP_001341502.1:p.Thr202=