Canonical Allele Identifier: CA626914123
Gene: APOH HGNC NCBI

Linked Data

dbSNP Id: rs1489315898
gnomAD v2: 17-64235761-CCA-C
gnomAD v3: 17-66239643-CCA-C
gnomAD v4: 17-66239643-CCA-C
MyVariant Identifiers: chr17:g.64235762_64235763del (hg19) chr17:g.66239644_66239645del (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.66239644_66239645del , CM000679.2:g.66239644_66239645del GRCh38
NC_000017.10:g.64235762_64235763del , CM000679.1:g.64235762_64235763del GRCh37
NC_000017.9:g.61666224_61666225del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000577982.1:c.-43-10223_-43-10222del ENSP00000464301.1:n.-43-10223_-43-10222del
Search 100 bp 5'
Search 100 bp 3'