Canonical Allele Identifier: CA437357889

Gene: AHSG

Linked Data

• MyVariant Identifiers: chr3:g.186336381T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.186618592T>G , CM000665.2:g.186618592T>G	GRCh38
NC_000003.11:g.186336381T>G , CM000665.1:g.186336381T>G	GRCh37
NC_000003.10:g.187819075T>G	NCBI36
NG_011436.1:g.10532T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000411641.7:c.630T>G MANE Select	ENSP00000393887.2:p.Ala210=
ENST00000273784.5:c.633T>G	ENSP00000273784.5:p.Ala211=
ENST00000411641.6:c.630T>G	ENSP00000393887.2:p.Ala210=
NM_001622.2:c.630T>G	NP_001613.2:p.Ala210=
NM_001354571.1:c.633T>G	NP_001341500.1:p.Ala211=
NM_001354572.1:c.627T>G	NP_001341501.1:p.Ala209=
NM_001354573.1:c.630T>G	NP_001341502.1:p.Ala210=
NM_001622.3:c.630T>G	NP_001613.2:p.Ala210=
NM_001622.4:c.630T>G MANE Select	NP_001613.2:p.Ala210=
NM_001354571.2:c.633T>G	NP_001341500.1:p.Ala211=
NM_001354572.2:c.627T>G	NP_001341501.1:p.Ala209=
NM_001354573.2:c.630T>G	NP_001341502.1:p.Ala210=