Canonical Allele Identifier: CA293120789

Gene: APOH

Linked Data

• dbSNP Id: rs958549564
• gnomAD v2: 17-64236390-A-C
• MyVariant Identifiers: chr17:g.64236390A>C (hg19) ; chr17:g.66240272A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.66240272A>C , CM000679.2:g.66240272A>C	GRCh38
NC_000017.10:g.64236390A>C , CM000679.1:g.64236390A>C	GRCh37
NC_000017.9:g.61666852A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000577982.1:c.-43-10850T>G	ENSP00000464301.1:n.-43-10850T>G