Canonical Allele Identifier: CA89626331

Gene: AHSG

Linked Data

• dbSNP Id: rs1047164291
• MyVariant Identifiers: chr3:g.186618314T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.186618314T>A , CM000665.2:g.186618314T>A	GRCh38
NC_000003.11:g.186336103T>A , CM000665.1:g.186336103T>A	GRCh37
NC_000003.10:g.187818797T>A	NCBI36
NG_011436.1:g.10254T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000411641.7:c.574-222T>A MANE Select	ENSP00000393887.2:n.574-222T>A
ENST00000273784.5:c.577-222T>A	ENSP00000273784.5:n.577-222T>A
ENST00000411641.6:c.574-222T>A	ENSP00000393887.2:n.574-222T>A
NM_001622.2:c.574-222T>A	NP_001613.2:n.574-222T>A
NM_001354571.1:c.577-222T>A	NP_001341500.1:n.577-222T>A
NM_001354572.1:c.571-222T>A	NP_001341501.1:n.571-222T>A
NM_001354573.1:c.574-222T>A	NP_001341502.1:n.574-222T>A
NM_001622.3:c.574-222T>A	NP_001613.2:n.574-222T>A
NM_001622.4:c.574-222T>A MANE Select	NP_001613.2:n.574-222T>A
NM_001354571.2:c.577-222T>A	NP_001341500.1:n.577-222T>A
NM_001354572.2:c.571-222T>A	NP_001341501.1:n.571-222T>A
NM_001354573.2:c.574-222T>A	NP_001341502.1:n.574-222T>A