Canonical Allele Identifier: CA985616635

Gene: APOH

Linked Data

• dbSNP Id: rs2073510724
• gnomAD v3: 17-66239584-C-T
• gnomAD v4: 17-66239584-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.66239584C>T , CM000679.2:g.66239584C>T	GRCh38
NC_000017.10:g.64235702C>T , CM000679.1:g.64235702C>T	GRCh37
NC_000017.9:g.61666164C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000577982.1:c.-43-10162G>A	ENSP00000464301.1:n.-43-10162G>A