Canonical Allele Identifier: CA2271191867

Gene: APOH

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.66228178T= , CM000679.2:g.66228178T=	GRCh38
NC_000017.10:g.64224296T= , CM000679.1:g.64224296T=	GRCh37
NC_000017.9:g.61654758T=	NCBI36
NG_012045.1:g.6261A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000205948.11:c.83A= MANE Select	ENSP00000205948.6:p.Asp28=
ENST00000205948.10:c.83A=	ENSP00000205948.6:p.Asp28=
ENST00000577982.1:c.83A=	ENSP00000464301.1:p.Asp28=
ENST00000581797.5:c.-98A=	ENSP00000463553.1:n.-98A=
NM_000042.2:c.83A=	NP_000033.2:p.Asp28=
NM_000042.3:c.83A= MANE Select	NP_000033.2:p.Asp28=