Canonical Allele Identifier: CA2668956784

Gene: AHSG

Linked Data

• gnomAD v4: 3-186620557-C-G

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.186620557C>G , CM000665.2:g.186620557C>G	GRCh38
NC_000003.11:g.186338346C>G , CM000665.1:g.186338346C>G	GRCh37
NC_000003.10:g.187821040C>G	NCBI36
NG_011436.1:g.12497C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000411641.7:c.760-29C>G MANE Select	ENSP00000393887.2:n.760-29C>G
ENST00000273784.5:c.763-29C>G	ENSP00000273784.5:n.763-29C>G
ENST00000411641.6:c.760-29C>G	ENSP00000393887.2:n.760-29C>G
NM_001622.2:c.760-29C>G	NP_001613.2:n.760-29C>G
NM_001354571.1:c.763-29C>G	NP_001341500.1:n.763-29C>G
NM_001354572.1:c.757-29C>G	NP_001341501.1:n.757-29C>G
NM_001354573.1:c.676-29C>G	NP_001341502.1:n.676-29C>G
NM_001622.3:c.760-29C>G	NP_001613.2:n.760-29C>G
NM_001622.4:c.760-29C>G MANE Select	NP_001613.2:n.760-29C>G
NM_001354571.2:c.763-29C>G	NP_001341500.1:n.763-29C>G
NM_001354572.2:c.757-29C>G	NP_001341501.1:n.757-29C>G
NM_001354573.2:c.676-29C>G	NP_001341502.1:n.676-29C>G