Canonical Allele Identifier: CA985616644

Gene: APOH

Linked Data

• dbSNP Id: rs2073510786
• gnomAD v3: 17-66239600-C-G
• gnomAD v4: 17-66239600-C-G

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.66239600C>G , CM000679.2:g.66239600C>G	GRCh38
NC_000017.10:g.64235718C>G , CM000679.1:g.64235718C>G	GRCh37
NC_000017.9:g.61666180C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000577982.1:c.-43-10178G>C	ENSP00000464301.1:n.-43-10178G>C