Canonical Allele Identifier: CA774239091

Gene: APOH

Linked Data

• dbSNP Id: rs1442103963
• MyVariant Identifiers: chr17:g.64235800A>G (hg19) ; chr17:g.66239682A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.66239682A>G , CM000679.2:g.66239682A>G	GRCh38
NC_000017.10:g.64235800A>G , CM000679.1:g.64235800A>G	GRCh37
NC_000017.9:g.61666262A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000577982.1:c.-43-10260T>C	ENSP00000464301.1:n.-43-10260T>C