Canonical Allele Identifier: CA2045510971

Gene: TPH2

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.71943065A= , CM000674.2:g.71943065A=	GRCh38
NC_000012.11:g.72336845A= , CM000674.1:g.72336845A=	GRCh37
NC_000012.10:g.70623112A=	NCBI36
NG_008279.1:g.9220A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000333850.4:c.256-1229A= MANE Select	ENSP00000329093.3:n.256-1229A=
ENST00000333850.3:c.256-1229A=	ENSP00000329093.3:n.256-1229A=
ENST00000546576.1:n.266-1229A=
NM_173353.3:c.256-1229A=	NP_775489.2:n.256-1229A=
XR_245894.2:n.356-1229A=
XR_001748575.1:n.356-1229A=
NM_173353.4:c.256-1229A= MANE Select	NP_775489.2:n.256-1229A=