Canonical Allele Identifier: CA2045565030

Gene: TPH2

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.72020942C= , CM000674.2:g.72020942C=	GRCh38
NC_000012.11:g.72414722C= , CM000674.1:g.72414722C=	GRCh37
NC_000012.10:g.70700989C=	NCBI36
NG_008279.1:g.87097C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333850.4:c.1069-1457C= MANE Select	ENSP00000329093.3:n.1069-1457C=
ENST00000333850.3:c.1069-1457C=	ENSP00000329093.3:n.1069-1457C=
NM_173353.3:c.1069-1457C=	NP_775489.2:n.1069-1457C=
XM_011537899.1:c.475-1457C=	XP_011536201.1:n.475-1457C=
NM_173353.4:c.1069-1457C= MANE Select	NP_775489.2:n.1069-1457C=