Canonical Allele Identifier: CA2045528133

Gene: TPH2

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.71983420C= , CM000674.2:g.71983420C=	GRCh38
NC_000012.11:g.72377200C= , CM000674.1:g.72377200C=	GRCh37
NC_000012.10:g.70663467C=	NCBI36
NG_008279.1:g.49575C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333850.4:c.941+4333C= MANE Select	ENSP00000329093.3:n.941+4333C=
ENST00000333850.3:c.941+4333C=	ENSP00000329093.3:n.941+4333C=
NM_173353.3:c.941+4333C=	NP_775489.2:n.941+4333C=
XM_011537899.1:c.347+4333C=	XP_011536201.1:n.347+4333C=
NM_173353.4:c.941+4333C= MANE Select	NP_775489.2:n.941+4333C=