Canonical Allele Identifier: CA355715610

Gene: AHSG

Linked Data

• MyVariant Identifiers: chr3:g.186338437C>G (hg19) ; chr3:g.186620648C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.186620648C>G , CM000665.2:g.186620648C>G	GRCh38
NC_000003.11:g.186338437C>G , CM000665.1:g.186338437C>G	GRCh37
NC_000003.10:g.187821131C>G	NCBI36
NG_011436.1:g.12588C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000411641.7:c.822C>G MANE Select	ENSP00000393887.2:p.Asp274Glu
ENST00000273784.5:c.825C>G	ENSP00000273784.5:p.Asp275Glu
ENST00000411641.6:c.822C>G	ENSP00000393887.2:p.Asp274Glu
NM_001622.2:c.822C>G	NP_001613.2:p.Asp274Glu
NM_001354571.1:c.825C>G	NP_001341500.1:p.Asp275Glu
NM_001354572.1:c.819C>G	NP_001341501.1:p.Asp273Glu
NM_001354573.1:c.738C>G	NP_001341502.1:p.Asp246Glu
NM_001622.3:c.822C>G	NP_001613.2:p.Asp274Glu
NM_001622.4:c.822C>G MANE Select	NP_001613.2:p.Asp274Glu
NM_001354571.2:c.825C>G	NP_001341500.1:p.Asp275Glu
NM_001354572.2:c.819C>G	NP_001341501.1:p.Asp273Glu
NM_001354573.2:c.738C>G	NP_001341502.1:p.Asp246Glu