Canonical Allele Identifier: CA626914132

Gene: APOH

Linked Data

• dbSNP Id: rs1418087366
• gnomAD v2: 17-64235816-A-G
• gnomAD v3: 17-66239698-A-G
• gnomAD v4: 17-66239698-A-G
• MyVariant Identifiers: chr17:g.64235816A>G (hg19) ; chr17:g.66239698A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.66239698A>G , CM000679.2:g.66239698A>G	GRCh38
NC_000017.10:g.64235816A>G , CM000679.1:g.64235816A>G	GRCh37
NC_000017.9:g.61666278A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000577982.1:c.-43-10276T>C	ENSP00000464301.1:n.-43-10276T>C