Canonical Allele Identifier: CA355714577

Gene: AHSG

Linked Data

• MyVariant Identifiers: chr3:g.186336398C>T (hg19) ; chr3:g.186618609C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.186618609C>T , CM000665.2:g.186618609C>T	GRCh38
NC_000003.11:g.186336398C>T , CM000665.1:g.186336398C>T	GRCh37
NC_000003.10:g.187819092C>T	NCBI36
NG_011436.1:g.10549C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000411641.7:c.647C>T MANE Select	ENSP00000393887.2:p.Ala216Val
ENST00000273784.5:c.650C>T	ENSP00000273784.5:p.Ala217Val
ENST00000411641.6:c.647C>T	ENSP00000393887.2:p.Ala216Val
NM_001622.2:c.647C>T	NP_001613.2:p.Ala216Val
NM_001354571.1:c.650C>T	NP_001341500.1:p.Ala217Val
NM_001354572.1:c.644C>T	NP_001341501.1:p.Ala215Val
NM_001354573.1:c.647C>T	NP_001341502.1:p.Ala216Val
NM_001622.3:c.647C>T	NP_001613.2:p.Ala216Val
NM_001622.4:c.647C>T MANE Select	NP_001613.2:p.Ala216Val
NM_001354571.2:c.650C>T	NP_001341500.1:p.Ala217Val
NM_001354572.2:c.644C>T	NP_001341501.1:p.Ala215Val
NM_001354573.2:c.647C>T	NP_001341502.1:p.Ala216Val