Canonical Allele Identifier: CA2271191742
Gene: APOH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.66227933A= , CM000679.2:g.66227933A= GRCh38
NC_000017.10:g.64224051A= , CM000679.1:g.64224051A= GRCh37
NC_000017.9:g.61654513A= NCBI36
NG_012045.1:g.6506T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000205948.11:c.241+87T= MANE Select ENSP00000205948.6:n.241+87T=
ENST00000205948.10:c.241+87T= ENSP00000205948.6:n.241+87T=
ENST00000577982.1:c.241+87T= ENSP00000464301.1:n.241+87T=
ENST00000581797.5:c.61+87T= ENSP00000463553.1:n.61+87T=
NM_000042.2:c.241+87T= NP_000033.2:n.241+87T=
NM_000042.3:c.241+87T= MANE Select NP_000033.2:n.241+87T=