Canonical Allele Identifier: CA626914124
Gene: APOH HGNC NCBI

Linked Data

dbSNP Id: rs1217988531
gnomAD v2: 17-64235765-T-TGTGA
gnomAD v3: 17-66239647-T-TGTGA
gnomAD v4: 17-66239647-T-TGTGA
MyVariant Identifiers: chr17:g.64235765_64235766insGTGA (hg19) chr17:g.66239647_66239648insGTGA (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.66239649_66239652dup , CM000679.2:g.66239649_66239652dup GRCh38
NC_000017.10:g.64235767_64235770dup , CM000679.1:g.64235767_64235770dup GRCh37
NC_000017.9:g.61666229_61666232dup NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000577982.1:c.-43-10229_-43-10226dup ENSP00000464301.1:n.-43-10229_-43-10226dup
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