Canonical Allele Identifier: CA2271191826
Gene: APOH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.66228097T= , CM000679.2:g.66228097T= GRCh38
NC_000017.10:g.64224215T= , CM000679.1:g.64224215T= GRCh37
NC_000017.9:g.61654677T= NCBI36
NG_012045.1:g.6342A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000205948.11:c.164A= MANE Select ENSP00000205948.6:p.Tyr55=
ENST00000205948.10:c.164A= ENSP00000205948.6:p.Tyr55=
ENST00000577982.1:c.164A= ENSP00000464301.1:p.Tyr55=
ENST00000581797.5:c.-17A= ENSP00000463553.1:n.-17A=
NM_000042.2:c.164A= NP_000033.2:p.Tyr55=
NM_000042.3:c.164A= MANE Select NP_000033.2:p.Tyr55=