Canonical Allele Identifier: CA437358359

Gene: AHSG

Linked Data

• MyVariant Identifiers: chr3:g.186338428C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.186620639C>G , CM000665.2:g.186620639C>G	GRCh38
NC_000003.11:g.186338428C>G , CM000665.1:g.186338428C>G	GRCh37
NC_000003.10:g.187821122C>G	NCBI36
NG_011436.1:g.12579C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000411641.7:c.813C>G MANE Select	ENSP00000393887.2:p.Pro271=
ENST00000273784.5:c.816C>G	ENSP00000273784.5:p.Pro272=
ENST00000411641.6:c.813C>G	ENSP00000393887.2:p.Pro271=
NM_001622.2:c.813C>G	NP_001613.2:p.Pro271=
NM_001354571.1:c.816C>G	NP_001341500.1:p.Pro272=
NM_001354572.1:c.810C>G	NP_001341501.1:p.Pro270=
NM_001354573.1:c.729C>G	NP_001341502.1:p.Pro243=
NM_001622.3:c.813C>G	NP_001613.2:p.Pro271=
NM_001622.4:c.813C>G MANE Select	NP_001613.2:p.Pro271=
NM_001354571.2:c.816C>G	NP_001341500.1:p.Pro272=
NM_001354572.2:c.810C>G	NP_001341501.1:p.Pro270=
NM_001354573.2:c.729C>G	NP_001341502.1:p.Pro243=