Canonical Allele Identifier: CA2639419288
Gene: APOH HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.66227968del , CM000679.2:g.66227968del GRCh38
NC_000017.10:g.64224086del , CM000679.1:g.64224086del GRCh37
NC_000017.9:g.61654548del NCBI36
NG_012045.1:g.6474del

Transcript Alleles

HGVS Amino-acid Change
ENST00000205948.11:c.241+55del MANE Select ENSP00000205948.6:n.241+55del
ENST00000205948.10:c.241+55del ENSP00000205948.6:n.241+55del
ENST00000577982.1:c.241+55del ENSP00000464301.1:n.241+55del
ENST00000581797.5:c.61+55del ENSP00000463553.1:n.61+55del
NM_000042.2:c.241+55del NP_000033.2:n.241+55del
NM_000042.3:c.241+55del MANE Select NP_000033.2:n.241+55del