Canonical Allele Identifier: CA2045550694

Gene: TPH2

Linked Data

• dbSNP Id: rs1873080406

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.72010782_72010786del , CM000674.2:g.72010782_72010786del	GRCh38
NC_000012.11:g.72404562_72404566del , CM000674.1:g.72404562_72404566del	GRCh37
NC_000012.10:g.70690829_70690833del	NCBI36
NG_008279.1:g.76937_76941del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333850.4:c.1069-11617_1069-11613del MANE Select	ENSP00000329093.3:n.1069-11617_1069-11613del
ENST00000333850.3:c.1069-11617_1069-11613del	ENSP00000329093.3:n.1069-11617_1069-11613del
NM_173353.3:c.1069-11617_1069-11613del	NP_775489.2:n.1069-11617_1069-11613del
XM_011537899.1:c.475-11617_475-11613del	XP_011536201.1:n.475-11617_475-11613del
NM_173353.4:c.1069-11617_1069-11613del MANE Select	NP_775489.2:n.1069-11617_1069-11613del