Canonical Allele Identifier: CA2045510899

Gene: TPH2

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.71942989C= , CM000674.2:g.71942989C=	GRCh38
NC_000012.11:g.72336769C= , CM000674.1:g.72336769C=	GRCh37
NC_000012.10:g.70623036C=	NCBI36
NG_008279.1:g.9144C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333850.4:c.255+1256C= MANE Select	ENSP00000329093.3:n.255+1256C=
ENST00000333850.3:c.255+1256C=	ENSP00000329093.3:n.255+1256C=
ENST00000546576.1:n.265+1256C=
NM_173353.3:c.255+1256C=	NP_775489.2:n.255+1256C=
XR_245894.2:n.355+1256C=
XR_001748575.1:n.355+1256C=
NM_173353.4:c.255+1256C= MANE Select	NP_775489.2:n.255+1256C=