Canonical Allele Identifier: CA2271191720

Gene: APOH

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.66227899A= , CM000679.2:g.66227899A=	GRCh38
NC_000017.10:g.64224017A= , CM000679.1:g.64224017A=	GRCh37
NC_000017.9:g.61654479A=	NCBI36
NG_012045.1:g.6540T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000205948.11:c.241+121T= MANE Select	ENSP00000205948.6:n.241+121T=
ENST00000205948.10:c.241+121T=	ENSP00000205948.6:n.241+121T=
ENST00000577982.1:c.241+121T=	ENSP00000464301.1:n.241+121T=
ENST00000581797.5:c.61+121T=	ENSP00000463553.1:n.61+121T=
NM_000042.2:c.241+121T=	NP_000033.2:n.241+121T=
NM_000042.3:c.241+121T= MANE Select	NP_000033.2:n.241+121T=