Canonical Allele Identifier: CA2668959085

Gene: AHSG

Linked Data

• gnomAD v4: 3-186618758-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.186618758C>A , CM000665.2:g.186618758C>A	GRCh38
NC_000003.11:g.186336547C>A , CM000665.1:g.186336547C>A	GRCh37
NC_000003.10:g.187819241C>A	NCBI36
NG_011436.1:g.10698C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000411641.7:c.675+121C>A MANE Select	ENSP00000393887.2:n.675+121C>A
ENST00000273784.5:c.678+121C>A	ENSP00000273784.5:n.678+121C>A
ENST00000411641.6:c.675+121C>A	ENSP00000393887.2:n.675+121C>A
NM_001622.2:c.675+121C>A	NP_001613.2:n.675+121C>A
NM_001354571.1:c.678+121C>A	NP_001341500.1:n.678+121C>A
NM_001354572.1:c.672+121C>A	NP_001341501.1:n.672+121C>A
NM_001354573.1:c.675+121C>A	NP_001341502.1:n.675+121C>A
NM_001622.3:c.675+121C>A	NP_001613.2:n.675+121C>A
NM_001622.4:c.675+121C>A MANE Select	NP_001613.2:n.675+121C>A
NM_001354571.2:c.678+121C>A	NP_001341500.1:n.678+121C>A
NM_001354572.2:c.672+121C>A	NP_001341501.1:n.672+121C>A
NM_001354573.2:c.675+121C>A	NP_001341502.1:n.675+121C>A