Canonical Allele Identifier: CA2733956504
Gene: APOH HGNC NCBI

Linked Data

dbSNP Id: rs1353705867

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.66239977T>C , CM000679.2:g.66239977T>C GRCh38
NC_000017.10:g.64236095T>C , CM000679.1:g.64236095T>C GRCh37
NC_000017.9:g.61666557T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000577982.1:c.-43-10555A>G ENSP00000464301.1:n.-43-10555A>G