Canonical Allele Identifier: CA949097462
Gene: TPH2 HGNC NCBI

Linked Data

dbSNP Id: rs1873391338

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.72020834T>A , CM000674.2:g.72020834T>A GRCh38
NC_000012.11:g.72414614T>A , CM000674.1:g.72414614T>A GRCh37
NC_000012.10:g.70700881T>A NCBI36
NG_008279.1:g.86989T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000333850.4:c.1069-1565T>A MANE Select ENSP00000329093.3:n.1069-1565T>A
ENST00000333850.3:c.1069-1565T>A ENSP00000329093.3:n.1069-1565T>A
NM_173353.3:c.1069-1565T>A NP_775489.2:n.1069-1565T>A
XM_011537899.1:c.475-1565T>A XP_011536201.1:n.475-1565T>A
NM_173353.4:c.1069-1565T>A MANE Select NP_775489.2:n.1069-1565T>A