Canonical Allele Identifier: CA985616694

Gene: APOH

Linked Data

• dbSNP Id: rs546876493
• gnomAD v3: 17-66239824-G-C
• gnomAD v4: 17-66239824-G-C

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.66239824G>C , CM000679.2:g.66239824G>C	GRCh38
NC_000017.10:g.64235942G>C , CM000679.1:g.64235942G>C	GRCh37
NC_000017.9:g.61666404G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000577982.1:c.-43-10402C>G	ENSP00000464301.1:n.-43-10402C>G