Canonical Allele Identifier: CA2744748

Gene: AHSG

Linked Data

• dbSNP Id: rs745549244
• ExAC: 3:186330905 C / T
• gnomAD v2: 3-186330905-C-T
• gnomAD v4: 3-186613116-C-T
• MyVariant Identifiers: chr3:g.186330905C>T (hg19) ; chr3:g.186613116C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.186613116C>T , CM000665.2:g.186613116C>T	GRCh38
NC_000003.11:g.186330905C>T , CM000665.1:g.186330905C>T	GRCh37
NC_000003.10:g.187813599C>T	NCBI36
NG_011436.1:g.5056C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000411641.7:c.-26C>T MANE Select	ENSP00000393887.2:n.-26C>T
ENST00000273784.5:c.-26C>T	ENSP00000273784.5:n.-26C>T
ENST00000411641.6:c.-26C>T	ENSP00000393887.2:n.-26C>T
ENST00000478441.1:n.32C>T
NM_001622.2:c.-26C>T	NP_001613.2:n.-26C>T
NM_001354571.1:c.-26C>T	NP_001341500.1:n.-26C>T
NM_001354572.1:c.-26C>T	NP_001341501.1:n.-26C>T
NM_001354573.1:c.-26C>T	NP_001341502.1:n.-26C>T
NM_001622.3:c.-26C>T	NP_001613.2:n.-26C>T
NM_001622.4:c.-26C>T MANE Select	NP_001613.2:n.-26C>T
NM_001354571.2:c.-26C>T	NP_001341500.1:n.-26C>T
NM_001354572.2:c.-26C>T	NP_001341501.1:n.-26C>T
NM_001354573.2:c.-26C>T	NP_001341502.1:n.-26C>T