Canonical Allele Identifier: CA626914181
Gene: APOH HGNC NCBI

Linked Data

dbSNP Id: rs1307258359
gnomAD v2: 17-64236176-AAAG-A
gnomAD v3: 17-66240058-AAAG-A
gnomAD v4: 17-66240058-AAAG-A
MyVariant Identifiers: chr17:g.64236177_64236179del (hg19) chr17:g.66240059_66240061del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.66240066_66240068del , CM000679.2:g.66240066_66240068del GRCh38
NC_000017.10:g.64236184_64236186del , CM000679.1:g.64236184_64236186del GRCh37
NC_000017.9:g.61666646_61666648del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000577982.1:c.-43-10639_-43-10637del ENSP00000464301.1:n.-43-10639_-43-10637del
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