Canonical Allele Identifier: CA2045533096

Gene: TPH2

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.71994533G= , CM000674.2:g.71994533G=	GRCh38
NC_000012.11:g.72388313G= , CM000674.1:g.72388313G=	GRCh37
NC_000012.10:g.70674580G=	NCBI36
NG_008279.1:g.60688G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333850.4:c.1036G= MANE Select	ENSP00000329093.3:p.Ala346=
ENST00000333850.3:c.1036G=	ENSP00000329093.3:p.Ala346=
NM_173353.3:c.1036G=	NP_775489.2:p.Ala346=
XM_011537899.1:c.442G=	XP_011536201.1:p.Ala148=
NM_173353.4:c.1036G= MANE Select	NP_775489.2:p.Ala346=