Canonical Allele Identifier: CA774239079
Gene: APOH HGNC NCBI

Linked Data

dbSNP Id: rs1458549599
MyVariant Identifiers: chr17:g.64235787C>T (hg19) chr17:g.66239669C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.66239669C>T , CM000679.2:g.66239669C>T GRCh38
NC_000017.10:g.64235787C>T , CM000679.1:g.64235787C>T GRCh37
NC_000017.9:g.61666249C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000577982.1:c.-43-10247G>A ENSP00000464301.1:n.-43-10247G>A
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