Canonical Allele Identifier: CA774239406

Gene: APOH

Linked Data

• dbSNP Id: rs2013785
• gnomAD v3: 17-66240359-A-T
• gnomAD v4: 17-66240359-A-T
• MyVariant Identifiers: chr17:g.64236477A>T (hg19) ; chr17:g.66240359A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.66240359A>T , CM000679.2:g.66240359A>T	GRCh38
NC_000017.10:g.64236477A>T , CM000679.1:g.64236477A>T	GRCh37
NC_000017.9:g.61666939A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000577982.1:c.-43-10937T>A	ENSP00000464301.1:n.-43-10937T>A