Canonical Allele Identifier: CA14384437
Gene: APOH HGNC NCBI

Linked Data

dbSNP Id: rs2013785
gnomAD v2: 17-64236477-A-G
gnomAD v3: 17-66240359-A-G
gnomAD v4: 17-66240359-A-G
MyVariant Identifiers: chr17:g.64236477A>G (hg19) chr17:g.66240359A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.66240359A>G , CM000679.2:g.66240359A>G GRCh38
NC_000017.10:g.64236477A>G , CM000679.1:g.64236477A>G GRCh37
NC_000017.9:g.61666939A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000577982.1:c.-43-10937T>C ENSP00000464301.1:n.-43-10937T>C
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