Canonical Allele Identifier: CA2744735

Gene: AHSG

Linked Data

• dbSNP Id: rs768603482
• ExAC: 3:186330870 C / T
• gnomAD v2: 3-186330870-C-T
• gnomAD v4: 3-186613081-C-T
• MyVariant Identifiers: chr3:g.186330870C>T (hg19) ; chr3:g.186613081C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.186613081C>T , CM000665.2:g.186613081C>T	GRCh38
NC_000003.11:g.186330870C>T , CM000665.1:g.186330870C>T	GRCh37
NC_000003.10:g.187813564C>T	NCBI36
NG_011436.1:g.5021C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000411641.7:c.-61C>T MANE Select	ENSP00000393887.2:n.-61C>T
ENST00000273784.5:c.-61C>T	ENSP00000273784.5:n.-61C>T
ENST00000411641.6:c.-61C>T	ENSP00000393887.2:n.-61C>T
NM_001622.2:c.-61C>T	NP_001613.2:n.-61C>T
NM_001354571.1:c.-61C>T	NP_001341500.1:n.-61C>T
NM_001354572.1:c.-61C>T	NP_001341501.1:n.-61C>T
NM_001354573.1:c.-61C>T	NP_001341502.1:n.-61C>T
NM_001622.3:c.-61C>T	NP_001613.2:n.-61C>T
NM_001622.4:c.-61C>T MANE Select	NP_001613.2:n.-61C>T
NM_001354571.2:c.-61C>T	NP_001341500.1:n.-61C>T
NM_001354572.2:c.-61C>T	NP_001341501.1:n.-61C>T
NM_001354573.2:c.-61C>T	NP_001341502.1:n.-61C>T