Canonical Allele Identifier: CA355715615

Gene: AHSG

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid change
ENST00000411641.7:c.824C>T MANE Select	ENSP00000393887.2:p.Pro275Leu
ENST00000273784.5:c.827C>T	ENSP00000273784.5:p.Pro276Leu
ENST00000411641.6:c.824C>T	ENSP00000393887.2:p.Pro275Leu
NM_001622.2:c.824C>T	NP_001613.2:p.Pro275Leu
NM_001354571.1:c.827C>T	NP_001341500.1:p.Pro276Leu
NM_001354572.1:c.821C>T	NP_001341501.1:p.Pro274Leu
NM_001354573.1:c.740C>T	NP_001341502.1:p.Pro247Leu
NM_001622.3:c.824C>T	NP_001613.2:p.Pro275Leu
NM_001622.4:c.824C>T MANE Select	NP_001613.2:p.Pro275Leu
NM_001354571.2:c.827C>T	NP_001341500.1:p.Pro276Leu
NM_001354572.2:c.821C>T	NP_001341501.1:p.Pro274Leu
NM_001354573.2:c.740C>T	NP_001341502.1:p.Pro247Leu