Canonical Allele Identifier: CA774239226
Gene: APOH HGNC NCBI

Linked Data

dbSNP Id: rs1464109239
MyVariant Identifiers: chr17:g.64236100G>A (hg19) chr17:g.66239982G>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.66239982G>A , CM000679.2:g.66239982G>A GRCh38
NC_000017.10:g.64236100G>A , CM000679.1:g.64236100G>A GRCh37
NC_000017.9:g.61666562G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000577982.1:c.-43-10560C>T ENSP00000464301.1:n.-43-10560C>T
Search 100 bp 5'
Search 100 bp 3'