Canonical Allele Identifier: CA2271184988

Gene: APOH

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.66214463T= , CM000679.2:g.66214463T=	GRCh38
NC_000017.10:g.64210581T= , CM000679.1:g.64210581T=	GRCh37
NC_000017.9:g.61641043T=	NCBI36
NG_012045.1:g.19976A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000205948.11:c.972A= MANE Select	ENSP00000205948.6:p.Lys324=
ENST00000205948.10:c.972A=	ENSP00000205948.6:p.Lys324=
ENST00000585162.1:c.258-2275A=
NM_000042.2:c.972A=	NP_000033.2:p.Lys324=
NM_000042.3:c.972A= MANE Select	NP_000033.2:p.Lys324=