Canonical Allele Identifier: CA355714595

Gene: AHSG

Linked Data

• MyVariant Identifiers: chr3:g.186336407G>T (hg19) ; chr3:g.186618618G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.186618618G>T , CM000665.2:g.186618618G>T	GRCh38
NC_000003.11:g.186336407G>T , CM000665.1:g.186336407G>T	GRCh37
NC_000003.10:g.187819101G>T	NCBI36
NG_011436.1:g.10558G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000411641.7:c.656G>T MANE Select	ENSP00000393887.2:p.Cys219Phe
ENST00000273784.5:c.659G>T	ENSP00000273784.5:p.Cys220Phe
ENST00000411641.6:c.656G>T	ENSP00000393887.2:p.Cys219Phe
NM_001622.2:c.656G>T	NP_001613.2:p.Cys219Phe
NM_001354571.1:c.659G>T	NP_001341500.1:p.Cys220Phe
NM_001354572.1:c.653G>T	NP_001341501.1:p.Cys218Phe
NM_001354573.1:c.656G>T	NP_001341502.1:p.Cys219Phe
NM_001622.3:c.656G>T	NP_001613.2:p.Cys219Phe
NM_001622.4:c.656G>T MANE Select	NP_001613.2:p.Cys219Phe
NM_001354571.2:c.659G>T	NP_001341500.1:p.Cys220Phe
NM_001354572.2:c.653G>T	NP_001341501.1:p.Cys218Phe
NM_001354573.2:c.656G>T	NP_001341502.1:p.Cys219Phe