Canonical Allele Identifier: CA2271191863
Gene: APOH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.66228168A= , CM000679.2:g.66228168A= GRCh38
NC_000017.10:g.64224286A= , CM000679.1:g.64224286A= GRCh37
NC_000017.9:g.61654748A= NCBI36
NG_012045.1:g.6271T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000205948.11:c.93T= MANE Select ENSP00000205948.6:p.Phe31=
ENST00000205948.10:c.93T= ENSP00000205948.6:p.Phe31=
ENST00000577982.1:c.93T= ENSP00000464301.1:p.Phe31=
ENST00000581797.5:c.-88T= ENSP00000463553.1:n.-88T=
NM_000042.2:c.93T= NP_000033.2:p.Phe31=
NM_000042.3:c.93T= MANE Select NP_000033.2:p.Phe31=