Canonical Allele Identifier: CA2639419331
Gene: APOH HGNC NCBI

Linked Data

gnomAD v4: 17-66228258-AGCCC-A
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.66228259_66228262del , CM000679.2:g.66228259_66228262del GRCh38
NC_000017.10:g.64224377_64224380del , CM000679.1:g.64224377_64224380del GRCh37
NC_000017.9:g.61654839_61654842del NCBI36
NG_012045.1:g.6177_6180del

Transcript Alleles

HGVS Amino-acid Change
ENST00000205948.11:c.65-66_65-63del MANE Select ENSP00000205948.6:n.65-66_65-63del
ENST00000205948.10:c.65-66_65-63del ENSP00000205948.6:n.65-66_65-63del
ENST00000577982.1:c.65-66_65-63del ENSP00000464301.1:n.65-66_65-63del
ENST00000581797.5:c.-116-66_-116-63del ENSP00000463553.1:n.-116-66_-116-63del
NM_000042.2:c.65-66_65-63del NP_000033.2:n.65-66_65-63del
NM_000042.3:c.65-66_65-63del MANE Select NP_000033.2:n.65-66_65-63del
Search 100 bp 5'
Search 100 bp 3'