Canonical Allele Identifier: CA2639419308
Gene: APOH HGNC NCBI

Linked Data

gnomAD v4: 17-66228145-GTTT-G
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.66228148_66228150del , CM000679.2:g.66228148_66228150del GRCh38
NC_000017.10:g.64224266_64224268del , CM000679.1:g.64224266_64224268del GRCh37
NC_000017.9:g.61654728_61654730del NCBI36
NG_012045.1:g.6291_6293del

Transcript Alleles

HGVS Amino-acid Change
ENST00000205948.11:c.113_115del MANE Select ENSP00000205948.6:p.Lys38del
ENST00000205948.10:c.113_115del ENSP00000205948.6:p.Lys38del
ENST00000577982.1:c.113_115del ENSP00000464301.1:p.Lys38del
ENST00000581797.5:c.-68_-66del ENSP00000463553.1:n.-68_-66del
NM_000042.2:c.113_115del NP_000033.2:p.Lys38del
NM_000042.3:c.113_115del MANE Select NP_000033.2:p.Lys38del
Search 100 bp 5'
Search 100 bp 3'