Canonical Allele Identifier: CA2271191820
Gene: APOH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.66228085C= , CM000679.2:g.66228085C= GRCh38
NC_000017.10:g.64224203C= , CM000679.1:g.64224203C= GRCh37
NC_000017.9:g.61654665C= NCBI36
NG_012045.1:g.6354G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000205948.11:c.176G= MANE Select ENSP00000205948.6:p.Gly59=
ENST00000205948.10:c.176G= ENSP00000205948.6:p.Gly59=
ENST00000577982.1:c.176G= ENSP00000464301.1:p.Gly59=
ENST00000581797.5:c.-5G= ENSP00000463553.1:n.-5G=
NM_000042.2:c.176G= NP_000033.2:p.Gly59=
NM_000042.3:c.176G= MANE Select NP_000033.2:p.Gly59=