Canonical Allele Identifier: CA985616795
Gene: APOH HGNC NCBI

Linked Data

dbSNP Id: rs2073512765

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.66240161A>G , CM000679.2:g.66240161A>G GRCh38
NC_000017.10:g.64236279A>G , CM000679.1:g.64236279A>G GRCh37
NC_000017.9:g.61666741A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000577982.1:c.-43-10739T>C ENSP00000464301.1:n.-43-10739T>C