Canonical Allele Identifier: CA2271191871
Gene: APOH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.66228186C= , CM000679.2:g.66228186C= GRCh38
NC_000017.10:g.64224304C= , CM000679.1:g.64224304C= GRCh37
NC_000017.9:g.61654766C= NCBI36
NG_012045.1:g.6253G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000205948.11:c.75G= MANE Select ENSP00000205948.6:p.Lys25=
ENST00000205948.10:c.75G= ENSP00000205948.6:p.Lys25=
ENST00000577982.1:c.75G= ENSP00000464301.1:p.Lys25=
ENST00000581797.5:c.-106G= ENSP00000463553.1:n.-106G=
NM_000042.2:c.75G= NP_000033.2:p.Lys25=
NM_000042.3:c.75G= MANE Select NP_000033.2:p.Lys25=