Canonical Allele Identifier: CA903915434

Gene: AHSG

Linked Data

• dbSNP Id: rs759771156
• MyVariant Identifiers: chr3:g.186330882C>G (hg19) ; chr3:g.186613093C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.186613093C>G , CM000665.2:g.186613093C>G	GRCh38
NC_000003.11:g.186330882C>G , CM000665.1:g.186330882C>G	GRCh37
NC_000003.10:g.187813576C>G	NCBI36
NG_011436.1:g.5033C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000411641.7:c.-49C>G MANE Select	ENSP00000393887.2:n.-49C>G
ENST00000273784.5:c.-49C>G	ENSP00000273784.5:n.-49C>G
ENST00000411641.6:c.-49C>G	ENSP00000393887.2:n.-49C>G
ENST00000478441.1:n.9C>G
NM_001622.2:c.-49C>G	NP_001613.2:n.-49C>G
NM_001354571.1:c.-49C>G	NP_001341500.1:n.-49C>G
NM_001354572.1:c.-49C>G	NP_001341501.1:n.-49C>G
NM_001354573.1:c.-49C>G	NP_001341502.1:n.-49C>G
NM_001622.3:c.-49C>G	NP_001613.2:n.-49C>G
NM_001622.4:c.-49C>G MANE Select	NP_001613.2:n.-49C>G
NM_001354571.2:c.-49C>G	NP_001341500.1:n.-49C>G
NM_001354572.2:c.-49C>G	NP_001341501.1:n.-49C>G
NM_001354573.2:c.-49C>G	NP_001341502.1:n.-49C>G