Canonical Allele Identifier: CA89626855

Gene: AHSG

Linked Data

• dbSNP Id: rs1033933844
• gnomAD v2: 3-186336488-T-A
• gnomAD v3: 3-186618699-T-A
• gnomAD v4: 3-186618699-T-A
• MyVariant Identifiers: chr3:g.186336488T>A (hg19) ; chr3:g.186618699T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.186618699T>A , CM000665.2:g.186618699T>A	GRCh38
NC_000003.11:g.186336488T>A , CM000665.1:g.186336488T>A	GRCh37
NC_000003.10:g.187819182T>A	NCBI36
NG_011436.1:g.10639T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000411641.7:c.675+62T>A MANE Select	ENSP00000393887.2:n.675+62T>A
ENST00000273784.5:c.678+62T>A	ENSP00000273784.5:n.678+62T>A
ENST00000411641.6:c.675+62T>A	ENSP00000393887.2:n.675+62T>A
NM_001622.2:c.675+62T>A	NP_001613.2:n.675+62T>A
NM_001354571.1:c.678+62T>A	NP_001341500.1:n.678+62T>A
NM_001354572.1:c.672+62T>A	NP_001341501.1:n.672+62T>A
NM_001354573.1:c.675+62T>A	NP_001341502.1:n.675+62T>A
NM_001622.3:c.675+62T>A	NP_001613.2:n.675+62T>A
NM_001622.4:c.675+62T>A MANE Select	NP_001613.2:n.675+62T>A
NM_001354571.2:c.678+62T>A	NP_001341500.1:n.678+62T>A
NM_001354572.2:c.672+62T>A	NP_001341501.1:n.672+62T>A
NM_001354573.2:c.675+62T>A	NP_001341502.1:n.675+62T>A