Canonical Allele Identifier: CA239239513

Gene: TPH2

Linked Data

• dbSNP Id: rs373917612

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.72020658dup , CM000674.2:g.72020658dup	GRCh38
NC_000012.11:g.72414438dup , CM000674.1:g.72414438dup	GRCh37
NC_000012.10:g.70700705dup	NCBI36
NG_008279.1:g.86813dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000333850.4:c.1069-1741dup MANE Select	ENSP00000329093.3:n.1069-1741dup
ENST00000333850.3:c.1069-1741dup	ENSP00000329093.3:n.1069-1741dup
NM_173353.3:c.1069-1741dup	NP_775489.2:n.1069-1741dup
XM_011537899.1:c.475-1741dup	XP_011536201.1:n.475-1741dup
NM_173353.4:c.1069-1741dup MANE Select	NP_775489.2:n.1069-1741dup