Canonical Allele Identifier: CA2271197519

Gene: APOH

Linked Data

• dbSNP Id: rs2073511851

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.66239925C>G , CM000679.2:g.66239925C>G	GRCh38
NC_000017.10:g.64236043C>G , CM000679.1:g.64236043C>G	GRCh37
NC_000017.9:g.61666505C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000577982.1:c.-43-10503G>C	ENSP00000464301.1:n.-43-10503G>C