Canonical Allele Identifier: CA2271191857
Gene: APOH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.66228154G= , CM000679.2:g.66228154G= GRCh38
NC_000017.10:g.64224272G= , CM000679.1:g.64224272G= GRCh37
NC_000017.9:g.61654734G= NCBI36
NG_012045.1:g.6285C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000205948.11:c.107C= MANE Select ENSP00000205948.6:p.Pro36=
ENST00000205948.10:c.107C= ENSP00000205948.6:p.Pro36=
ENST00000577982.1:c.107C= ENSP00000464301.1:p.Pro36=
ENST00000581797.5:c.-74C= ENSP00000463553.1:n.-74C=
NM_000042.2:c.107C= NP_000033.2:p.Pro36=
NM_000042.3:c.107C= MANE Select NP_000033.2:p.Pro36=