Canonical Allele Identifier: CA548458855

Gene: AHSG

Linked Data

• dbSNP Id: rs1319893111
• gnomAD v2: 3-186330880-C-T
• MyVariant Identifiers: chr3:g.186330880C>T (hg19) ; chr3:g.186613091C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.186613091C>T , CM000665.2:g.186613091C>T	GRCh38
NC_000003.11:g.186330880C>T , CM000665.1:g.186330880C>T	GRCh37
NC_000003.10:g.187813574C>T	NCBI36
NG_011436.1:g.5031C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000411641.7:c.-51C>T MANE Select	ENSP00000393887.2:n.-51C>T
ENST00000273784.5:c.-51C>T	ENSP00000273784.5:n.-51C>T
ENST00000411641.6:c.-51C>T	ENSP00000393887.2:n.-51C>T
ENST00000478441.1:n.7C>T
NM_001622.2:c.-51C>T	NP_001613.2:n.-51C>T
NM_001354571.1:c.-51C>T	NP_001341500.1:n.-51C>T
NM_001354572.1:c.-51C>T	NP_001341501.1:n.-51C>T
NM_001354573.1:c.-51C>T	NP_001341502.1:n.-51C>T
NM_001622.3:c.-51C>T	NP_001613.2:n.-51C>T
NM_001622.4:c.-51C>T MANE Select	NP_001613.2:n.-51C>T
NM_001354571.2:c.-51C>T	NP_001341500.1:n.-51C>T
NM_001354572.2:c.-51C>T	NP_001341501.1:n.-51C>T
NM_001354573.2:c.-51C>T	NP_001341502.1:n.-51C>T