Canonical Allele Identifier: CA355715602

Gene: AHSG

Linked Data

• gnomAD v4: 3-186620644-T-G
• MyVariant Identifiers: chr3:g.186338433T>G (hg19) ; chr3:g.186620644T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.186620644T>G , CM000665.2:g.186620644T>G	GRCh38
NC_000003.11:g.186338433T>G , CM000665.1:g.186338433T>G	GRCh37
NC_000003.10:g.187821127T>G	NCBI36
NG_011436.1:g.12584T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000411641.7:c.818T>G MANE Select	ENSP00000393887.2:p.Val273Gly
ENST00000273784.5:c.821T>G	ENSP00000273784.5:p.Val274Gly
ENST00000411641.6:c.818T>G	ENSP00000393887.2:p.Val273Gly
NM_001622.2:c.818T>G	NP_001613.2:p.Val273Gly
NM_001354571.1:c.821T>G	NP_001341500.1:p.Val274Gly
NM_001354572.1:c.815T>G	NP_001341501.1:p.Val272Gly
NM_001354573.1:c.734T>G	NP_001341502.1:p.Val245Gly
NM_001622.3:c.818T>G	NP_001613.2:p.Val273Gly
NM_001622.4:c.818T>G MANE Select	NP_001613.2:p.Val273Gly
NM_001354571.2:c.821T>G	NP_001341500.1:p.Val274Gly
NM_001354572.2:c.815T>G	NP_001341501.1:p.Val272Gly
NM_001354573.2:c.734T>G	NP_001341502.1:p.Val245Gly