Canonical Allele Identifier: CA2271191864

Gene: APOH

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.66228171T= , CM000679.2:g.66228171T=	GRCh38
NC_000017.10:g.64224289T= , CM000679.1:g.64224289T=	GRCh37
NC_000017.9:g.61654751T=	NCBI36
NG_012045.1:g.6268A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000205948.11:c.90A= MANE Select	ENSP00000205948.6:p.Pro30=
ENST00000205948.10:c.90A=	ENSP00000205948.6:p.Pro30=
ENST00000577982.1:c.90A=	ENSP00000464301.1:p.Pro30=
ENST00000581797.5:c.-91A=	ENSP00000463553.1:n.-91A=
NM_000042.2:c.90A=	NP_000033.2:p.Pro30=
NM_000042.3:c.90A= MANE Select	NP_000033.2:p.Pro30=