Canonical Allele Identifier: CA2271197386
Gene: APOH HGNC NCBI

Linked Data

dbSNP Id: rs2073511357

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.66239785dup , CM000679.2:g.66239785dup GRCh38
NC_000017.10:g.64235903dup , CM000679.1:g.64235903dup GRCh37
NC_000017.9:g.61666365dup NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000577982.1:c.-43-10359dup ENSP00000464301.1:n.-43-10359dup