Canonical Allele Identifier: CA89626468

Gene: AHSG

Linked Data

• dbSNP Id: rs923748932
• gnomAD v3: 3-186618406-A-G
• gnomAD v4: 3-186618406-A-G
• MyVariant Identifiers: chr3:g.186336195A>G (hg19) ; chr3:g.186618406A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.186618406A>G , CM000665.2:g.186618406A>G	GRCh38
NC_000003.11:g.186336195A>G , CM000665.1:g.186336195A>G	GRCh37
NC_000003.10:g.187818889A>G	NCBI36
NG_011436.1:g.10346A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000411641.7:c.574-130A>G MANE Select	ENSP00000393887.2:n.574-130A>G
ENST00000273784.5:c.577-130A>G	ENSP00000273784.5:n.577-130A>G
ENST00000411641.6:c.574-130A>G	ENSP00000393887.2:n.574-130A>G
NM_001622.2:c.574-130A>G	NP_001613.2:n.574-130A>G
NM_001354571.1:c.577-130A>G	NP_001341500.1:n.577-130A>G
NM_001354572.1:c.571-130A>G	NP_001341501.1:n.571-130A>G
NM_001354573.1:c.574-130A>G	NP_001341502.1:n.574-130A>G
NM_001622.3:c.574-130A>G	NP_001613.2:n.574-130A>G
NM_001622.4:c.574-130A>G MANE Select	NP_001613.2:n.574-130A>G
NM_001354571.2:c.577-130A>G	NP_001341500.1:n.577-130A>G
NM_001354572.2:c.571-130A>G	NP_001341501.1:n.571-130A>G
NM_001354573.2:c.574-130A>G	NP_001341502.1:n.574-130A>G