Canonical Allele Identifier: CA355715614

Gene: AHSG

Linked Data

• MyVariant Identifiers: chr3:g.186338439C>G (hg19) ; chr3:g.186620650C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.186620650C>G , CM000665.2:g.186620650C>G	GRCh38
NC_000003.11:g.186338439C>G , CM000665.1:g.186338439C>G	GRCh37
NC_000003.10:g.187821133C>G	NCBI36
NG_011436.1:g.12590C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000411641.7:c.824C>G MANE Select	ENSP00000393887.2:p.Pro275Arg
ENST00000273784.5:c.827C>G	ENSP00000273784.5:p.Pro276Arg
ENST00000411641.6:c.824C>G	ENSP00000393887.2:p.Pro275Arg
NM_001622.2:c.824C>G	NP_001613.2:p.Pro275Arg
NM_001354571.1:c.827C>G	NP_001341500.1:p.Pro276Arg
NM_001354572.1:c.821C>G	NP_001341501.1:p.Pro274Arg
NM_001354573.1:c.740C>G	NP_001341502.1:p.Pro247Arg
NM_001622.3:c.824C>G	NP_001613.2:p.Pro275Arg
NM_001622.4:c.824C>G MANE Select	NP_001613.2:p.Pro275Arg
NM_001354571.2:c.827C>G	NP_001341500.1:p.Pro276Arg
NM_001354572.2:c.821C>G	NP_001341501.1:p.Pro274Arg
NM_001354573.2:c.740C>G	NP_001341502.1:p.Pro247Arg