Canonical Allele Identifier: CA355714616

Gene: AHSG

Linked Data

• MyVariant Identifiers: chr3:g.186336418G>A (hg19) ; chr3:g.186618629G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.186618629G>A , CM000665.2:g.186618629G>A	GRCh38
NC_000003.11:g.186336418G>A , CM000665.1:g.186336418G>A	GRCh37
NC_000003.10:g.187819112G>A	NCBI36
NG_011436.1:g.10569G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000411641.7:c.667G>A MANE Select	ENSP00000393887.2:p.Ala223Thr
ENST00000273784.5:c.670G>A	ENSP00000273784.5:p.Ala224Thr
ENST00000411641.6:c.667G>A	ENSP00000393887.2:p.Ala223Thr
NM_001622.2:c.667G>A	NP_001613.2:p.Ala223Thr
NM_001354571.1:c.670G>A	NP_001341500.1:p.Ala224Thr
NM_001354572.1:c.664G>A	NP_001341501.1:p.Ala222Thr
NM_001354573.1:c.667G>A	NP_001341502.1:p.Ala223Thr
NM_001622.3:c.667G>A	NP_001613.2:p.Ala223Thr
NM_001622.4:c.667G>A MANE Select	NP_001613.2:p.Ala223Thr
NM_001354571.2:c.670G>A	NP_001341500.1:p.Ala224Thr
NM_001354572.2:c.664G>A	NP_001341501.1:p.Ala222Thr
NM_001354573.2:c.667G>A	NP_001341502.1:p.Ala223Thr