Canonical Allele Identifier: CA293120698

Gene: APOH

Linked Data

• dbSNP Id: rs10048208
• gnomAD v2: 17-64236042-G-A
• gnomAD v3: 17-66239924-G-A
• gnomAD v4: 17-66239924-G-A
• MyVariant Identifiers: chr17:g.64236042G>A (hg19) ; chr17:g.66239924G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.66239924G>A , CM000679.2:g.66239924G>A	GRCh38
NC_000017.10:g.64236042G>A , CM000679.1:g.64236042G>A	GRCh37
NC_000017.9:g.61666504G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000577982.1:c.-43-10502C>T	ENSP00000464301.1:n.-43-10502C>T