Canonical Allele Identifier: CA2271191880

Gene: APOH

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.66228220G= , CM000679.2:g.66228220G=	GRCh38
NC_000017.10:g.64224338G= , CM000679.1:g.64224338G=	GRCh37
NC_000017.9:g.61654800G=	NCBI36
NG_012045.1:g.6219C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000205948.11:c.65-24C= MANE Select	ENSP00000205948.6:n.65-24C=
ENST00000205948.10:c.65-24C=	ENSP00000205948.6:n.65-24C=
ENST00000577982.1:c.65-24C=	ENSP00000464301.1:n.65-24C=
ENST00000581797.5:c.-116-24C=	ENSP00000463553.1:n.-116-24C=
NM_000042.2:c.65-24C=	NP_000033.2:n.65-24C=
NM_000042.3:c.65-24C= MANE Select	NP_000033.2:n.65-24C=