Canonical Allele Identifier: CA774233498
Gene: APOH HGNC NCBI

Linked Data

dbSNP Id: rs1193435703
MyVariant Identifiers: chr17:g.64227312G>A (hg19) chr17:g.66231194G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.66231194G>A , CM000679.2:g.66231194G>A GRCh38
NC_000017.10:g.64227312G>A , CM000679.1:g.64227312G>A GRCh37
NC_000017.9:g.61657774G>A NCBI36
NG_012045.1:g.3245C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000577982.1:c.-43-1772C>T ENSP00000464301.1:n.-43-1772C>T
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