Canonical Allele Identifier: CA985616847
Gene: APOH HGNC NCBI

Linked Data

dbSNP Id: rs2073513373
gnomAD v3: 17-66240333-G-C
gnomAD v4: 17-66240333-G-C
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.66240333G>C , CM000679.2:g.66240333G>C GRCh38
NC_000017.10:g.64236451G>C , CM000679.1:g.64236451G>C GRCh37
NC_000017.9:g.61666913G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000577982.1:c.-43-10911C>G ENSP00000464301.1:n.-43-10911C>G
Search 100 bp 5'
Search 100 bp 3'