Canonical Allele Identifier: CA691603903
Gene: TPH2 HGNC NCBI

Linked Data

dbSNP Id: rs1265358104

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.72020730G>T , CM000674.2:g.72020730G>T GRCh38
NC_000012.11:g.72414510G>T , CM000674.1:g.72414510G>T GRCh37
NC_000012.10:g.70700777G>T NCBI36
NG_008279.1:g.86885G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000333850.4:c.1069-1669G>T MANE Select ENSP00000329093.3:n.1069-1669G>T
ENST00000333850.3:c.1069-1669G>T ENSP00000329093.3:n.1069-1669G>T
NM_173353.3:c.1069-1669G>T NP_775489.2:n.1069-1669G>T
XM_011537899.1:c.475-1669G>T XP_011536201.1:n.475-1669G>T
NM_173353.4:c.1069-1669G>T MANE Select NP_775489.2:n.1069-1669G>T