Canonical Allele Identifier: CA355714529

Gene: AHSG

Linked Data

• MyVariant Identifiers: chr3:g.186336377T>A (hg19) ; chr3:g.186618588T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.186618588T>A , CM000665.2:g.186618588T>A	GRCh38
NC_000003.11:g.186336377T>A , CM000665.1:g.186336377T>A	GRCh37
NC_000003.10:g.187819071T>A	NCBI36
NG_011436.1:g.10528T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000411641.7:c.626T>A MANE Select	ENSP00000393887.2:p.Val209Asp
ENST00000273784.5:c.629T>A	ENSP00000273784.5:p.Val210Asp
ENST00000411641.6:c.626T>A	ENSP00000393887.2:p.Val209Asp
NM_001622.2:c.626T>A	NP_001613.2:p.Val209Asp
NM_001354571.1:c.629T>A	NP_001341500.1:p.Val210Asp
NM_001354572.1:c.623T>A	NP_001341501.1:p.Val208Asp
NM_001354573.1:c.626T>A	NP_001341502.1:p.Val209Asp
NM_001622.3:c.626T>A	NP_001613.2:p.Val209Asp
NM_001622.4:c.626T>A MANE Select	NP_001613.2:p.Val209Asp
NM_001354571.2:c.629T>A	NP_001341500.1:p.Val210Asp
NM_001354572.2:c.623T>A	NP_001341501.1:p.Val208Asp
NM_001354573.2:c.626T>A	NP_001341502.1:p.Val209Asp