Canonical Allele Identifier: CA355714506

Gene: AHSG

Linked Data

• MyVariant Identifiers: chr3:g.186336367A>G (hg19) ; chr3:g.186618578A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.186618578A>G , CM000665.2:g.186618578A>G	GRCh38
NC_000003.11:g.186336367A>G , CM000665.1:g.186336367A>G	GRCh37
NC_000003.10:g.187819061A>G	NCBI36
NG_011436.1:g.10518A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000411641.7:c.616A>G MANE Select	ENSP00000393887.2:p.Thr206Ala
ENST00000273784.5:c.619A>G	ENSP00000273784.5:p.Thr207Ala
ENST00000411641.6:c.616A>G	ENSP00000393887.2:p.Thr206Ala
NM_001622.2:c.616A>G	NP_001613.2:p.Thr206Ala
NM_001354571.1:c.619A>G	NP_001341500.1:p.Thr207Ala
NM_001354572.1:c.613A>G	NP_001341501.1:p.Thr205Ala
NM_001354573.1:c.616A>G	NP_001341502.1:p.Thr206Ala
NM_001622.3:c.616A>G	NP_001613.2:p.Thr206Ala
NM_001622.4:c.616A>G MANE Select	NP_001613.2:p.Thr206Ala
NM_001354571.2:c.619A>G	NP_001341500.1:p.Thr207Ala
NM_001354572.2:c.613A>G	NP_001341501.1:p.Thr205Ala
NM_001354573.2:c.616A>G	NP_001341502.1:p.Thr206Ala