Canonical Allele Identifier: CA2271197253
Gene: APOH HGNC NCBI

Linked Data

dbSNP Id: rs1598558649
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.66239612T>A , CM000679.2:g.66239612T>A GRCh38
NC_000017.10:g.64235730T>A , CM000679.1:g.64235730T>A GRCh37
NC_000017.9:g.61666192T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000577982.1:c.-43-10190A>T ENSP00000464301.1:n.-43-10190A>T
Search 100 bp 5'
Search 100 bp 3'