Canonical Allele Identifier: CA2045510772

Gene: TPH2

Linked Data

• dbSNP Id: rs1871110434

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.71942871T>G , CM000674.2:g.71942871T>G	GRCh38
NC_000012.11:g.72336651T>G , CM000674.1:g.72336651T>G	GRCh37
NC_000012.10:g.70622918T>G	NCBI36
NG_008279.1:g.9026T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333850.4:c.255+1138T>G MANE Select	ENSP00000329093.3:n.255+1138T>G
ENST00000333850.3:c.255+1138T>G	ENSP00000329093.3:n.255+1138T>G
ENST00000546576.1:n.265+1138T>G
NM_173353.3:c.255+1138T>G	NP_775489.2:n.255+1138T>G
XR_245894.2:n.355+1138T>G
XR_001748575.1:n.355+1138T>G
NM_173353.4:c.255+1138T>G MANE Select	NP_775489.2:n.255+1138T>G