Canonical Allele Identifier: CA774239335
Gene: APOH HGNC NCBI

Linked Data

dbSNP Id: rs1176708695
MyVariant Identifiers: chr17:g.64236215A>G (hg19) chr17:g.66240097A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.66240097A>G , CM000679.2:g.66240097A>G GRCh38
NC_000017.10:g.64236215A>G , CM000679.1:g.64236215A>G GRCh37
NC_000017.9:g.61666677A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000577982.1:c.-43-10675T>C ENSP00000464301.1:n.-43-10675T>C
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