Canonical Allele Identifier: CA2271191865

Gene: APOH

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.66228173G= , CM000679.2:g.66228173G=	GRCh38
NC_000017.10:g.64224291G= , CM000679.1:g.64224291G=	GRCh37
NC_000017.9:g.61654753G=	NCBI36
NG_012045.1:g.6266C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000205948.11:c.88C= MANE Select	ENSP00000205948.6:p.Pro30=
ENST00000205948.10:c.88C=	ENSP00000205948.6:p.Pro30=
ENST00000577982.1:c.88C=	ENSP00000464301.1:p.Pro30=
ENST00000581797.5:c.-93C=	ENSP00000463553.1:n.-93C=
NM_000042.2:c.88C=	NP_000033.2:p.Pro30=
NM_000042.3:c.88C= MANE Select	NP_000033.2:p.Pro30=