Canonical Allele Identifier: CA2271191836
Gene: APOH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.66228111G= , CM000679.2:g.66228111G= GRCh38
NC_000017.10:g.64224229G= , CM000679.1:g.64224229G= GRCh37
NC_000017.9:g.61654691G= NCBI36
NG_012045.1:g.6328C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000205948.11:c.150C= MANE Select ENSP00000205948.6:p.Ser50=
ENST00000205948.10:c.150C= ENSP00000205948.6:p.Ser50=
ENST00000577982.1:c.150C= ENSP00000464301.1:p.Ser50=
ENST00000581797.5:c.-31C= ENSP00000463553.1:n.-31C=
NM_000042.2:c.150C= NP_000033.2:p.Ser50=
NM_000042.3:c.150C= MANE Select NP_000033.2:p.Ser50=