Canonical Allele Identifier: CA2271191821
Gene: APOH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.66228087T= , CM000679.2:g.66228087T= GRCh38
NC_000017.10:g.64224205T= , CM000679.1:g.64224205T= GRCh37
NC_000017.9:g.61654667T= NCBI36
NG_012045.1:g.6352A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000205948.11:c.174A= MANE Select ENSP00000205948.6:p.Arg58=
ENST00000205948.10:c.174A= ENSP00000205948.6:p.Arg58=
ENST00000577982.1:c.174A= ENSP00000464301.1:p.Arg58=
ENST00000581797.5:c.-7A= ENSP00000463553.1:n.-7A=
NM_000042.2:c.174A= NP_000033.2:p.Arg58=
NM_000042.3:c.174A= MANE Select NP_000033.2:p.Arg58=