Canonical Allele Identifier: CA2271197602
Gene: APOH HGNC NCBI

Linked Data

dbSNP Id: rs2073512410
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.66240055A>T , CM000679.2:g.66240055A>T GRCh38
NC_000017.10:g.64236173A>T , CM000679.1:g.64236173A>T GRCh37
NC_000017.9:g.61666635A>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000577982.1:c.-43-10633T>A ENSP00000464301.1:n.-43-10633T>A
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