Canonical Allele Identifier: CA437358373

Gene: AHSG

Linked Data

• dbSNP Id: rs1460703567
• gnomAD v2: 3-186338434-G-A
• gnomAD v3: 3-186620645-G-A
• gnomAD v4: 3-186620645-G-A
• MyVariant Identifiers: chr3:g.186338434G>A (hg19) ; chr3:g.186620645G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.186620645G>A , CM000665.2:g.186620645G>A	GRCh38
NC_000003.11:g.186338434G>A , CM000665.1:g.186338434G>A	GRCh37
NC_000003.10:g.187821128G>A	NCBI36
NG_011436.1:g.12585G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000411641.7:c.819G>A MANE Select	ENSP00000393887.2:p.Val273=
ENST00000273784.5:c.822G>A	ENSP00000273784.5:p.Val274=
ENST00000411641.6:c.819G>A	ENSP00000393887.2:p.Val273=
NM_001622.2:c.819G>A	NP_001613.2:p.Val273=
NM_001354571.1:c.822G>A	NP_001341500.1:p.Val274=
NM_001354572.1:c.816G>A	NP_001341501.1:p.Val272=
NM_001354573.1:c.735G>A	NP_001341502.1:p.Val245=
NM_001622.3:c.819G>A	NP_001613.2:p.Val273=
NM_001622.4:c.819G>A MANE Select	NP_001613.2:p.Val273=
NM_001354571.2:c.822G>A	NP_001341500.1:p.Val274=
NM_001354572.2:c.816G>A	NP_001341501.1:p.Val272=
NM_001354573.2:c.735G>A	NP_001341502.1:p.Val245=