Canonical Allele Identifier: CA2739826605

Gene: AHSG

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.186613086T>C , CM000665.2:g.186613086T>C	GRCh38
NC_000003.11:g.186330875T>C , CM000665.1:g.186330875T>C	GRCh37
NC_000003.10:g.187813569T>C	NCBI36
NG_011436.1:g.5026T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000411641.7:c.-56T>C MANE Select	ENSP00000393887.2:n.-56T>C
ENST00000273784.5:c.-56T>C	ENSP00000273784.5:n.-56T>C
ENST00000411641.6:c.-56T>C	ENSP00000393887.2:n.-56T>C
ENST00000478441.1:n.2T>C
NM_001622.2:c.-56T>C	NP_001613.2:n.-56T>C
NM_001354571.1:c.-56T>C	NP_001341500.1:n.-56T>C
NM_001354572.1:c.-56T>C	NP_001341501.1:n.-56T>C
NM_001354573.1:c.-56T>C	NP_001341502.1:n.-56T>C
NM_001622.3:c.-56T>C	NP_001613.2:n.-56T>C
NM_001622.4:c.-56T>C MANE Select	NP_001613.2:n.-56T>C
NM_001354571.2:c.-56T>C	NP_001341500.1:n.-56T>C
NM_001354572.2:c.-56T>C	NP_001341501.1:n.-56T>C
NM_001354573.2:c.-56T>C	NP_001341502.1:n.-56T>C