Canonical Allele Identifier: CA2271197553

Gene: APOH

Linked Data

• dbSNP Id: rs2073512062

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.66239962A>G , CM000679.2:g.66239962A>G	GRCh38
NC_000017.10:g.64236080A>G , CM000679.1:g.64236080A>G	GRCh37
NC_000017.9:g.61666542A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000577982.1:c.-43-10540T>C	ENSP00000464301.1:n.-43-10540T>C