Canonical Allele Identifier: CA293120628
Gene: APOH HGNC NCBI

Linked Data

dbSNP Id: rs937143504
MyVariant Identifiers: chr17:g.64235765T>C (hg19) chr17:g.66239647T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.66239647T>C , CM000679.2:g.66239647T>C GRCh38
NC_000017.10:g.64235765T>C , CM000679.1:g.64235765T>C GRCh37
NC_000017.9:g.61666227T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000577982.1:c.-43-10225A>G ENSP00000464301.1:n.-43-10225A>G
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