Canonical Allele Identifier: CA293120757

Gene: APOH

Linked Data

• dbSNP Id: rs550977060
• gnomAD v3: 17-66240127-A-C
• gnomAD v4: 17-66240127-A-C
• MyVariant Identifiers: chr17:g.64236245A>C (hg19) ; chr17:g.66240127A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.66240127A>C , CM000679.2:g.66240127A>C	GRCh38
NC_000017.10:g.64236245A>C , CM000679.1:g.64236245A>C	GRCh37
NC_000017.9:g.61666707A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000577982.1:c.-43-10705T>G	ENSP00000464301.1:n.-43-10705T>G