Canonical Allele Identifier: CA2045533094

Gene: TPH2

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.71994531G= , CM000674.2:g.71994531G=	GRCh38
NC_000012.11:g.72388311G= , CM000674.1:g.72388311G=	GRCh37
NC_000012.10:g.70674578G=	NCBI36
NG_008279.1:g.60686G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000333850.4:c.1034G= MANE Select	ENSP00000329093.3:p.Gly345=
ENST00000333850.3:c.1034G=	ENSP00000329093.3:p.Gly345=
NM_173353.3:c.1034G=	NP_775489.2:p.Gly345=
XM_011537899.1:c.440G=	XP_011536201.1:p.Gly147=
NM_173353.4:c.1034G= MANE Select	NP_775489.2:p.Gly345=