Canonical Allele Identifier: CA985616816

Gene: APOH

Linked Data

• dbSNP Id: rs2073512985
• gnomAD v3: 17-66240215-T-C
• gnomAD v4: 17-66240215-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.66240215T>C , CM000679.2:g.66240215T>C	GRCh38
NC_000017.10:g.64236333T>C , CM000679.1:g.64236333T>C	GRCh37
NC_000017.9:g.61666795T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000577982.1:c.-43-10793A>G	ENSP00000464301.1:n.-43-10793A>G