Canonical Allele Identifier: CA914198770
Gene: APOH HGNC NCBI

Linked Data

dbSNP Id: rs1567746507

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.66240236T>C , CM000679.2:g.66240236T>C GRCh38
NC_000017.10:g.64236354T>C , CM000679.1:g.64236354T>C GRCh37
NC_000017.9:g.61666816T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000577982.1:c.-43-10814A>G ENSP00000464301.1:n.-43-10814A>G