Canonical Allele Identifier: CA501476634

Gene: APOH

Linked Data

• dbSNP Id: rs1194175492
• gnomAD v3: 17-66239923-C-T
• gnomAD v4: 17-66239923-C-T
• MyVariant Identifiers: chr17:g.64236041C>T (hg19) ; chr17:g.66239923C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.66239923C>T , CM000679.2:g.66239923C>T	GRCh38
NC_000017.10:g.64236041C>T , CM000679.1:g.64236041C>T	GRCh37
NC_000017.9:g.61666503C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000577982.1:c.-43-10501G>A	ENSP00000464301.1:n.-43-10501G>A