Canonical Allele Identifier: CA2739826610

Gene: AHSG

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.186613092C>A , CM000665.2:g.186613092C>A	GRCh38
NC_000003.11:g.186330881C>A , CM000665.1:g.186330881C>A	GRCh37
NC_000003.10:g.187813575C>A	NCBI36
NG_011436.1:g.5032C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000411641.7:c.-50C>A MANE Select	ENSP00000393887.2:n.-50C>A
ENST00000273784.5:c.-50C>A	ENSP00000273784.5:n.-50C>A
ENST00000411641.6:c.-50C>A	ENSP00000393887.2:n.-50C>A
ENST00000478441.1:n.8C>A
NM_001622.2:c.-50C>A	NP_001613.2:n.-50C>A
NM_001354571.1:c.-50C>A	NP_001341500.1:n.-50C>A
NM_001354572.1:c.-50C>A	NP_001341501.1:n.-50C>A
NM_001354573.1:c.-50C>A	NP_001341502.1:n.-50C>A
NM_001622.3:c.-50C>A	NP_001613.2:n.-50C>A
NM_001622.4:c.-50C>A MANE Select	NP_001613.2:n.-50C>A
NM_001354571.2:c.-50C>A	NP_001341500.1:n.-50C>A
NM_001354572.2:c.-50C>A	NP_001341501.1:n.-50C>A
NM_001354573.2:c.-50C>A	NP_001341502.1:n.-50C>A