Canonical Allele Identifier: CA903916668

Gene: AHSG

Linked Data

• dbSNP Id: rs1277980280
• MyVariant Identifiers: chr3:g.186332593C>T (hg19) ; chr3:g.186614804C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.186614804C>T , CM000665.2:g.186614804C>T	GRCh38
NC_000003.11:g.186332593C>T , CM000665.1:g.186332593C>T	GRCh37
NC_000003.10:g.187815287C>T	NCBI36
NG_011436.1:g.6744C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000411641.7:c.214-881C>T MANE Select	ENSP00000393887.2:n.214-881C>T
ENST00000273784.5:c.214-881C>T	ENSP00000273784.5:n.214-881C>T
ENST00000411641.6:c.214-881C>T	ENSP00000393887.2:n.214-881C>T
ENST00000478441.1:n.271-881C>T
NM_001622.2:c.214-881C>T	NP_001613.2:n.214-881C>T
NM_001354571.1:c.214-881C>T	NP_001341500.1:n.214-881C>T
NM_001354572.1:c.214-884C>T	NP_001341501.1:n.214-884C>T
NM_001354573.1:c.214-881C>T	NP_001341502.1:n.214-881C>T
NM_001622.3:c.214-881C>T	NP_001613.2:n.214-881C>T
NM_001622.4:c.214-881C>T MANE Select	NP_001613.2:n.214-881C>T
NM_001354571.2:c.214-881C>T	NP_001341500.1:n.214-881C>T
NM_001354572.2:c.214-884C>T	NP_001341501.1:n.214-884C>T
NM_001354573.2:c.214-881C>T	NP_001341502.1:n.214-881C>T