Canonical Allele Identifier: CA2639419347
Gene: APOH HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.66228288dup , CM000679.2:g.66228288dup GRCh38
NC_000017.10:g.64224406dup , CM000679.1:g.64224406dup GRCh37
NC_000017.9:g.61654868dup NCBI36
NG_012045.1:g.6151dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000205948.11:c.65-92dup MANE Select ENSP00000205948.6:n.65-92dup
ENST00000205948.10:c.65-92dup ENSP00000205948.6:n.65-92dup
ENST00000577982.1:c.65-92dup ENSP00000464301.1:n.65-92dup
ENST00000581797.5:c.-116-92dup ENSP00000463553.1:n.-116-92dup
NM_000042.2:c.65-92dup NP_000033.2:n.65-92dup
NM_000042.3:c.65-92dup MANE Select NP_000033.2:n.65-92dup