Canonical Allele Identifier: CA2045551142

Gene: TPH2

Linked Data

• dbSNP Id: rs1873088419

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.72011105G>C , CM000674.2:g.72011105G>C	GRCh38
NC_000012.11:g.72404885G>C , CM000674.1:g.72404885G>C	GRCh37
NC_000012.10:g.70691152G>C	NCBI36
NG_008279.1:g.77260G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333850.4:c.1069-11294G>C MANE Select	ENSP00000329093.3:n.1069-11294G>C
ENST00000333850.3:c.1069-11294G>C	ENSP00000329093.3:n.1069-11294G>C
NM_173353.3:c.1069-11294G>C	NP_775489.2:n.1069-11294G>C
XM_011537899.1:c.475-11294G>C	XP_011536201.1:n.475-11294G>C
NM_173353.4:c.1069-11294G>C MANE Select	NP_775489.2:n.1069-11294G>C