Canonical Allele Identifier: CA2271191852
Gene: APOH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.66228145G= , CM000679.2:g.66228145G= GRCh38
NC_000017.10:g.64224263G= , CM000679.1:g.64224263G= GRCh37
NC_000017.9:g.61654725G= NCBI36
NG_012045.1:g.6294C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000205948.11:c.116C= MANE Select ENSP00000205948.6:p.Thr39=
ENST00000205948.10:c.116C= ENSP00000205948.6:p.Thr39=
ENST00000577982.1:c.116C= ENSP00000464301.1:p.Thr39=
ENST00000581797.5:c.-65C= ENSP00000463553.1:n.-65C=
NM_000042.2:c.116C= NP_000033.2:p.Thr39=
NM_000042.3:c.116C= MANE Select NP_000033.2:p.Thr39=