Canonical Allele Identifier: CA985616641
Gene: APOH HGNC NCBI

Linked Data

dbSNP Id: rs528705064
gnomAD v3: 17-66239599-T-G
gnomAD v4: 17-66239599-T-G
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Genomic Alleles

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

Transcript Alleles

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