Canonical Allele Identifier: CA293120707
Gene: APOH HGNC NCBI

Linked Data

dbSNP Id: rs1032805544
MyVariant Identifiers: chr17:g.64236067A>G (hg19) chr17:g.66239949A>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.66239949A>G , CM000679.2:g.66239949A>G GRCh38
NC_000017.10:g.64236067A>G , CM000679.1:g.64236067A>G GRCh37
NC_000017.9:g.61666529A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000577982.1:c.-43-10527T>C ENSP00000464301.1:n.-43-10527T>C
Search 100 bp 5'
Search 100 bp 3'