Canonical Allele Identifier: CA2271197014

Gene: APOH

Linked Data

• dbSNP Id: rs2073512707
• gnomAD v3: 17-66240140-T-G
• gnomAD v4: 17-66240140-T-G

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.66240140T>G , CM000679.2:g.66240140T>G	GRCh38
NC_000017.10:g.64236258T>G , CM000679.1:g.64236258T>G	GRCh37
NC_000017.9:g.61666720T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000577982.1:c.-43-10718A>C	ENSP00000464301.1:n.-43-10718A>C