Canonical Allele Identifier: CA985616846
Gene: APOH HGNC NCBI

Linked Data

dbSNP Id: rs1598558772

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.66240331T>G , CM000679.2:g.66240331T>G GRCh38
NC_000017.10:g.64236449T>G , CM000679.1:g.64236449T>G GRCh37
NC_000017.9:g.61666911T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000577982.1:c.-43-10909A>C ENSP00000464301.1:n.-43-10909A>C