Canonical Allele Identifier: CA355714502

Gene: AHSG

Linked Data

• MyVariant Identifiers: chr3:g.186336364G>C (hg19) ; chr3:g.186618575G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.186618575G>C , CM000665.2:g.186618575G>C	GRCh38
NC_000003.11:g.186336364G>C , CM000665.1:g.186336364G>C	GRCh37
NC_000003.10:g.187819058G>C	NCBI36
NG_011436.1:g.10515G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000411641.7:c.613G>C MANE Select	ENSP00000393887.2:p.Gly205Arg
ENST00000273784.5:c.616G>C	ENSP00000273784.5:p.Gly206Arg
ENST00000411641.6:c.613G>C	ENSP00000393887.2:p.Gly205Arg
NM_001622.2:c.613G>C	NP_001613.2:p.Gly205Arg
NM_001354571.1:c.616G>C	NP_001341500.1:p.Gly206Arg
NM_001354572.1:c.610G>C	NP_001341501.1:p.Gly204Arg
NM_001354573.1:c.613G>C	NP_001341502.1:p.Gly205Arg
NM_001622.3:c.613G>C	NP_001613.2:p.Gly205Arg
NM_001622.4:c.613G>C MANE Select	NP_001613.2:p.Gly205Arg
NM_001354571.2:c.616G>C	NP_001341500.1:p.Gly206Arg
NM_001354572.2:c.610G>C	NP_001341501.1:p.Gly204Arg
NM_001354573.2:c.613G>C	NP_001341502.1:p.Gly205Arg