Canonical Allele Identifier: CA2271197269
Gene: APOH HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.66239643_66239645delinsCCA , CM000679.2:g.66239643_66239645delinsCCA GRCh38
NC_000017.10:g.64235761_64235763delinsCCA , CM000679.1:g.64235761_64235763delinsCCA GRCh37
NC_000017.9:g.61666223_61666225delinsCCA NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000577982.1:c.-43-10223_-43-10221delinsTGG ENSP00000464301.1:n.-43-10223_-43-10221delinsTGG
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