Canonical Allele Identifier: CA2668956793

Gene: AHSG

Linked Data

• gnomAD v4: 3-186620570-A-C

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.186620570A>C , CM000665.2:g.186620570A>C	GRCh38
NC_000003.11:g.186338359A>C , CM000665.1:g.186338359A>C	GRCh37
NC_000003.10:g.187821053A>C	NCBI36
NG_011436.1:g.12510A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000411641.7:c.760-16A>C MANE Select	ENSP00000393887.2:n.760-16A>C
ENST00000273784.5:c.763-16A>C	ENSP00000273784.5:n.763-16A>C
ENST00000411641.6:c.760-16A>C	ENSP00000393887.2:n.760-16A>C
NM_001622.2:c.760-16A>C	NP_001613.2:n.760-16A>C
NM_001354571.1:c.763-16A>C	NP_001341500.1:n.763-16A>C
NM_001354572.1:c.757-16A>C	NP_001341501.1:n.757-16A>C
NM_001354573.1:c.676-16A>C	NP_001341502.1:n.676-16A>C
NM_001622.3:c.760-16A>C	NP_001613.2:n.760-16A>C
NM_001622.4:c.760-16A>C MANE Select	NP_001613.2:n.760-16A>C
NM_001354571.2:c.763-16A>C	NP_001341500.1:n.763-16A>C
NM_001354572.2:c.757-16A>C	NP_001341501.1:n.757-16A>C
NM_001354573.2:c.676-16A>C	NP_001341502.1:n.676-16A>C