Canonical Allele Identifier: CA2045510985

Gene: TPH2

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.71943075C= , CM000674.2:g.71943075C=	GRCh38
NC_000012.11:g.72336855C= , CM000674.1:g.72336855C=	GRCh37
NC_000012.10:g.70623122C=	NCBI36
NG_008279.1:g.9230C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333850.4:c.256-1219C= MANE Select	ENSP00000329093.3:n.256-1219C=
ENST00000333850.3:c.256-1219C=	ENSP00000329093.3:n.256-1219C=
ENST00000546576.1:n.266-1219C=
NM_173353.3:c.256-1219C=	NP_775489.2:n.256-1219C=
XR_245894.2:n.356-1219C=
XR_001748575.1:n.356-1219C=
NM_173353.4:c.256-1219C= MANE Select	NP_775489.2:n.256-1219C=