Canonical Allele Identifier: CA2271197352
Gene: APOH HGNC NCBI

Linked Data

dbSNP Id: rs2073511197

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.66239721T>C , CM000679.2:g.66239721T>C GRCh38
NC_000017.10:g.64235839T>C , CM000679.1:g.64235839T>C GRCh37
NC_000017.9:g.61666301T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000577982.1:c.-43-10299A>G ENSP00000464301.1:n.-43-10299A>G