Canonical Allele Identifier: CA2271191849
Gene: APOH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.66228135C= , CM000679.2:g.66228135C= GRCh38
NC_000017.10:g.64224253C= , CM000679.1:g.64224253C= GRCh37
NC_000017.9:g.61654715C= NCBI36
NG_012045.1:g.6304G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000205948.11:c.126G= MANE Select ENSP00000205948.6:p.Glu42=
ENST00000205948.10:c.126G= ENSP00000205948.6:p.Glu42=
ENST00000577982.1:c.126G= ENSP00000464301.1:p.Glu42=
ENST00000581797.5:c.-55G= ENSP00000463553.1:n.-55G=
NM_000042.2:c.126G= NP_000033.2:p.Glu42=
NM_000042.3:c.126G= MANE Select NP_000033.2:p.Glu42=