Canonical Allele Identifier: CA2271191878

Gene: APOH

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.66228211A= , CM000679.2:g.66228211A=	GRCh38
NC_000017.10:g.64224329A= , CM000679.1:g.64224329A=	GRCh37
NC_000017.9:g.61654791A=	NCBI36
NG_012045.1:g.6228T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000205948.11:c.65-15T= MANE Select	ENSP00000205948.6:n.65-15T=
ENST00000205948.10:c.65-15T=	ENSP00000205948.6:n.65-15T=
ENST00000577982.1:c.65-15T=	ENSP00000464301.1:n.65-15T=
ENST00000581797.5:c.-116-15T=	ENSP00000463553.1:n.-116-15T=
NM_000042.2:c.65-15T=	NP_000033.2:n.65-15T=
NM_000042.3:c.65-15T= MANE Select	NP_000033.2:n.65-15T=