Canonical Allele Identifier: CA626914120
Gene: APOH HGNC NCBI

Linked Data

dbSNP Id: rs528705064
gnomAD v2: 17-64235717-T-C
gnomAD v3: 17-66239599-T-C
gnomAD v4: 17-66239599-T-C
MyVariant Identifiers: chr17:g.64235717T>C (hg19) chr17:g.66239599T>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.66239599T>C , CM000679.2:g.66239599T>C GRCh38
NC_000017.10:g.64235717T>C , CM000679.1:g.64235717T>C GRCh37
NC_000017.9:g.61666179T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000577982.1:c.-43-10177A>G ENSP00000464301.1:n.-43-10177A>G
Search 100 bp 5'
Search 100 bp 3'