Canonical Allele Identifier: CA355714553

Gene: AHSG

Linked Data

• MyVariant Identifiers: chr3:g.186336387G>T (hg19) ; chr3:g.186618598G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.186618598G>T , CM000665.2:g.186618598G>T	GRCh38
NC_000003.11:g.186336387G>T , CM000665.1:g.186336387G>T	GRCh37
NC_000003.10:g.187819081G>T	NCBI36
NG_011436.1:g.10538G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000411641.7:c.636G>T MANE Select	ENSP00000393887.2:p.Glu212Asp
ENST00000273784.5:c.639G>T	ENSP00000273784.5:p.Glu213Asp
ENST00000411641.6:c.636G>T	ENSP00000393887.2:p.Glu212Asp
NM_001622.2:c.636G>T	NP_001613.2:p.Glu212Asp
NM_001354571.1:c.639G>T	NP_001341500.1:p.Glu213Asp
NM_001354572.1:c.633G>T	NP_001341501.1:p.Glu211Asp
NM_001354573.1:c.636G>T	NP_001341502.1:p.Glu212Asp
NM_001622.3:c.636G>T	NP_001613.2:p.Glu212Asp
NM_001622.4:c.636G>T MANE Select	NP_001613.2:p.Glu212Asp
NM_001354571.2:c.639G>T	NP_001341500.1:p.Glu213Asp
NM_001354572.2:c.633G>T	NP_001341501.1:p.Glu211Asp
NM_001354573.2:c.636G>T	NP_001341502.1:p.Glu212Asp