Canonical Allele Identifier: CA2759779270

Gene: AHSG

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.186617864C>A , CM000665.2:g.186617864C>A	GRCh38
NC_000003.11:g.186335653C>A , CM000665.1:g.186335653C>A	GRCh37
NC_000003.10:g.187818347C>A	NCBI36
NG_011436.1:g.9804C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000411641.7:c.573+514C>A MANE Select	ENSP00000393887.2:n.573+514C>A
ENST00000273784.5:c.576+514C>A	ENSP00000273784.5:n.576+514C>A
ENST00000411641.6:c.573+514C>A	ENSP00000393887.2:n.573+514C>A
ENST00000478441.1:n.1144C>A
NM_001622.2:c.573+514C>A	NP_001613.2:n.573+514C>A
NM_001354571.1:c.576+514C>A	NP_001341500.1:n.576+514C>A
NM_001354572.1:c.570+514C>A	NP_001341501.1:n.570+514C>A
NM_001354573.1:c.573+514C>A	NP_001341502.1:n.573+514C>A
NM_001622.3:c.573+514C>A	NP_001613.2:n.573+514C>A
NM_001622.4:c.573+514C>A MANE Select	NP_001613.2:n.573+514C>A
NM_001354571.2:c.576+514C>A	NP_001341500.1:n.576+514C>A
NM_001354572.2:c.570+514C>A	NP_001341501.1:n.570+514C>A
NM_001354573.2:c.573+514C>A	NP_001341502.1:n.573+514C>A