Canonical Allele Identifier: CA985616711
Gene: APOH HGNC NCBI

Linked Data

dbSNP Id: rs2073511758
gnomAD v3: 17-66239898-C-A
gnomAD v4: 17-66239898-C-A
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.66239898C>A , CM000679.2:g.66239898C>A GRCh38
NC_000017.10:g.64236016C>A , CM000679.1:g.64236016C>A GRCh37
NC_000017.9:g.61666478C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000577982.1:c.-43-10476G>T ENSP00000464301.1:n.-43-10476G>T
Search 100 bp 5'
Search 100 bp 3'