Canonical Allele Identifier: CA2045561888

Gene: TPH2

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.72018661C= , CM000674.2:g.72018661C=	GRCh38
NC_000012.11:g.72412441C= , CM000674.1:g.72412441C=	GRCh37
NC_000012.10:g.70698708C=	NCBI36
NG_008279.1:g.84816C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333850.4:c.1069-3738C= MANE Select	ENSP00000329093.3:n.1069-3738C=
ENST00000333850.3:c.1069-3738C=	ENSP00000329093.3:n.1069-3738C=
NM_173353.3:c.1069-3738C=	NP_775489.2:n.1069-3738C=
XM_011537899.1:c.475-3738C=	XP_011536201.1:n.475-3738C=
NM_173353.4:c.1069-3738C= MANE Select	NP_775489.2:n.1069-3738C=