Canonical Allele Identifier: CA293120631
Gene: APOH HGNC NCBI

Linked Data

dbSNP Id: rs539239297
gnomAD v2: 17-64235767-TGA-T
gnomAD v3: 17-66239649-TGA-T
gnomAD v4: 17-66239649-TGA-T
MyVariant Identifiers: chr17:g.64235768_64235769del (hg19) chr17:g.66239650_66239651del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.66239653_66239654del , CM000679.2:g.66239653_66239654del GRCh38
NC_000017.10:g.64235771_64235772del , CM000679.1:g.64235771_64235772del GRCh37
NC_000017.9:g.61666233_61666234del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000577982.1:c.-43-10229_-43-10228del ENSP00000464301.1:n.-43-10229_-43-10228del
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