Canonical Allele Identifier: CA626914183

Gene: APOH

Linked Data

• dbSNP Id: rs1457902248
• gnomAD v2: 17-64236221-T-C
• gnomAD v3: 17-66240103-T-C
• gnomAD v4: 17-66240103-T-C
• MyVariant Identifiers: chr17:g.64236221T>C (hg19) ; chr17:g.66240103T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.66240103T>C , CM000679.2:g.66240103T>C	GRCh38
NC_000017.10:g.64236221T>C , CM000679.1:g.64236221T>C	GRCh37
NC_000017.9:g.61666683T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000577982.1:c.-43-10681A>G	ENSP00000464301.1:n.-43-10681A>G