Canonical Allele Identifier: CA2271191733

Gene: APOH

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.66227916A= , CM000679.2:g.66227916A=	GRCh38
NC_000017.10:g.64224034A= , CM000679.1:g.64224034A=	GRCh37
NC_000017.9:g.61654496A=	NCBI36
NG_012045.1:g.6523T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000205948.11:c.241+104T= MANE Select	ENSP00000205948.6:n.241+104T=
ENST00000205948.10:c.241+104T=	ENSP00000205948.6:n.241+104T=
ENST00000577982.1:c.241+104T=	ENSP00000464301.1:n.241+104T=
ENST00000581797.5:c.61+104T=	ENSP00000463553.1:n.61+104T=
NM_000042.2:c.241+104T=	NP_000033.2:n.241+104T=
NM_000042.3:c.241+104T= MANE Select	NP_000033.2:n.241+104T=