Canonical Allele Identifier: CA2045533062

Gene: TPH2

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.71994439A= , CM000674.2:g.71994439A=	GRCh38
NC_000012.11:g.72388219A= , CM000674.1:g.72388219A=	GRCh37
NC_000012.10:g.70674486A=	NCBI36
NG_008279.1:g.60594A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000333850.4:c.942A= MANE Select	ENSP00000329093.3:p.Pro314=
ENST00000333850.3:c.942A=	ENSP00000329093.3:p.Pro314=
NM_173353.3:c.942A=	NP_775489.2:p.Pro314=
XM_011537899.1:c.348A=	XP_011536201.1:p.Pro116=
NM_173353.4:c.942A= MANE Select	NP_775489.2:p.Pro314=