Canonical Allele Identifier: CA2045533098

Gene: TPH2

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.71994538A= , CM000674.2:g.71994538A=	GRCh38
NC_000012.11:g.72388318A= , CM000674.1:g.72388318A=	GRCh37
NC_000012.10:g.70674585A=	NCBI36
NG_008279.1:g.60693A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000333850.4:c.1041A= MANE Select	ENSP00000329093.3:p.Ser347=
ENST00000333850.3:c.1041A=	ENSP00000329093.3:p.Ser347=
NM_173353.3:c.1041A=	NP_775489.2:p.Ser347=
XM_011537899.1:c.447A=	XP_011536201.1:p.Ser149=
NM_173353.4:c.1041A= MANE Select	NP_775489.2:p.Ser347=