Canonical Allele Identifier: CA2271191888

Gene: APOH

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.66228250T= , CM000679.2:g.66228250T=	GRCh38
NC_000017.10:g.64224368T= , CM000679.1:g.64224368T=	GRCh37
NC_000017.9:g.61654830T=	NCBI36
NG_012045.1:g.6189A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000205948.11:c.65-54A= MANE Select	ENSP00000205948.6:n.65-54A=
ENST00000205948.10:c.65-54A=	ENSP00000205948.6:n.65-54A=
ENST00000577982.1:c.65-54A=	ENSP00000464301.1:n.65-54A=
ENST00000581797.5:c.-116-54A=	ENSP00000463553.1:n.-116-54A=
NM_000042.2:c.65-54A=	NP_000033.2:n.65-54A=
NM_000042.3:c.65-54A= MANE Select	NP_000033.2:n.65-54A=