Canonical Allele Identifier: CA774239268
Gene: APOH HGNC NCBI

Linked Data

dbSNP Id: rs1328499497
MyVariant Identifiers: chr17:g.64236172A>C (hg19) chr17:g.66240054A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.66240054A>C , CM000679.2:g.66240054A>C GRCh38
NC_000017.10:g.64236172A>C , CM000679.1:g.64236172A>C GRCh37
NC_000017.9:g.61666634A>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000577982.1:c.-43-10632T>G ENSP00000464301.1:n.-43-10632T>G
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