Canonical Allele Identifier: CA437357976

Gene: AHSG

Linked Data

• MyVariant Identifiers: chr3:g.186336426G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.186618637G>A , CM000665.2:g.186618637G>A	GRCh38
NC_000003.11:g.186336426G>A , CM000665.1:g.186336426G>A	GRCh37
NC_000003.10:g.187819120G>A	NCBI36
NG_011436.1:g.10577G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000411641.7:c.675G>A MANE Select	ENSP00000393887.2:p.Lys225=
ENST00000273784.5:c.678G>A	ENSP00000273784.5:p.Lys226=
ENST00000411641.6:c.675G>A	ENSP00000393887.2:p.Lys225=
NM_001622.2:c.675G>A	NP_001613.2:p.Lys225=
NM_001354571.1:c.678G>A	NP_001341500.1:p.Lys226=
NM_001354572.1:c.672G>A	NP_001341501.1:p.Lys224=
NM_001354573.1:c.675G>A	NP_001341502.1:p.Lys225=
NM_001622.3:c.675G>A	NP_001613.2:p.Lys225=
NM_001622.4:c.675G>A MANE Select	NP_001613.2:p.Lys225=
NM_001354571.2:c.678G>A	NP_001341500.1:p.Lys226=
NM_001354572.2:c.672G>A	NP_001341501.1:p.Lys224=
NM_001354573.2:c.675G>A	NP_001341502.1:p.Lys225=