Canonical Allele Identifier: CA2271197303
Gene: APOH HGNC NCBI

Linked Data

dbSNP Id: rs2073511030
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.66239668C>T , CM000679.2:g.66239668C>T GRCh38
NC_000017.10:g.64235786C>T , CM000679.1:g.64235786C>T GRCh37
NC_000017.9:g.61666248C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000577982.1:c.-43-10246G>A ENSP00000464301.1:n.-43-10246G>A
Search 100 bp 5'
Search 100 bp 3'