Canonical Allele Identifier: CA2744976

Gene: AHSG

Linked Data

• dbSNP Id: rs766031984
• ExAC: 3:186336435 G / A
• gnomAD v2: 3-186336435-G-A
• gnomAD v3: 3-186618646-G-A
• gnomAD v4: 3-186618646-G-A
• MyVariant Identifiers: chr3:g.186336435G>A (hg19) ; chr3:g.186618646G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.186618646G>A , CM000665.2:g.186618646G>A	GRCh38
NC_000003.11:g.186336435G>A , CM000665.1:g.186336435G>A	GRCh37
NC_000003.10:g.187819129G>A	NCBI36
NG_011436.1:g.10586G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000411641.7:c.675+9G>A MANE Select	ENSP00000393887.2:n.675+9G>A
ENST00000273784.5:c.678+9G>A	ENSP00000273784.5:n.678+9G>A
ENST00000411641.6:c.675+9G>A	ENSP00000393887.2:n.675+9G>A
NM_001622.2:c.675+9G>A	NP_001613.2:n.675+9G>A
NM_001354571.1:c.678+9G>A	NP_001341500.1:n.678+9G>A
NM_001354572.1:c.672+9G>A	NP_001341501.1:n.672+9G>A
NM_001354573.1:c.675+9G>A	NP_001341502.1:n.675+9G>A
NM_001622.3:c.675+9G>A	NP_001613.2:n.675+9G>A
NM_001622.4:c.675+9G>A MANE Select	NP_001613.2:n.675+9G>A
NM_001354571.2:c.678+9G>A	NP_001341500.1:n.678+9G>A
NM_001354572.2:c.672+9G>A	NP_001341501.1:n.672+9G>A
NM_001354573.2:c.675+9G>A	NP_001341502.1:n.675+9G>A