Canonical Allele Identifier: CA2271191908
Gene: APOH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.66228287T= , CM000679.2:g.66228287T= GRCh38
NC_000017.10:g.64224405T= , CM000679.1:g.64224405T= GRCh37
NC_000017.9:g.61654867T= NCBI36
NG_012045.1:g.6152A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000205948.11:c.65-91A= MANE Select ENSP00000205948.6:n.65-91A=
ENST00000205948.10:c.65-91A= ENSP00000205948.6:n.65-91A=
ENST00000577982.1:c.65-91A= ENSP00000464301.1:n.65-91A=
ENST00000581797.5:c.-116-91A= ENSP00000463553.1:n.-116-91A=
NM_000042.2:c.65-91A= NP_000033.2:n.65-91A=
NM_000042.3:c.65-91A= MANE Select NP_000033.2:n.65-91A=