Canonical Allele Identifier: CA2271191918
Gene: APOH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.66228313A= , CM000679.2:g.66228313A= GRCh38
NC_000017.10:g.64224431A= , CM000679.1:g.64224431A= GRCh37
NC_000017.9:g.61654893A= NCBI36
NG_012045.1:g.6126T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000205948.11:c.65-117T= MANE Select ENSP00000205948.6:n.65-117T=
ENST00000205948.10:c.65-117T= ENSP00000205948.6:n.65-117T=
ENST00000577982.1:c.65-117T= ENSP00000464301.1:n.65-117T=
ENST00000581797.5:c.-116-117T= ENSP00000463553.1:n.-116-117T=
NM_000042.2:c.65-117T= NP_000033.2:n.65-117T=
NM_000042.3:c.65-117T= MANE Select NP_000033.2:n.65-117T=