Canonical Allele Identifier: CA2271184989

Gene: APOH

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.66214464T= , CM000679.2:g.66214464T=	GRCh38
NC_000017.10:g.64210582T= , CM000679.1:g.64210582T=	GRCh37
NC_000017.9:g.61641044T=	NCBI36
NG_012045.1:g.19975A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000205948.11:c.971A= MANE Select	ENSP00000205948.6:p.Lys324=
ENST00000205948.10:c.971A=	ENSP00000205948.6:p.Lys324=
ENST00000585162.1:c.258-2276A=
NM_000042.2:c.971A=	NP_000033.2:p.Lys324=
NM_000042.3:c.971A= MANE Select	NP_000033.2:p.Lys324=