Canonical Allele Identifier: CA691604016
Gene: TPH2 HGNC NCBI

Linked Data

dbSNP Id: rs1334829380

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.72020871del , CM000674.2:g.72020871del GRCh38
NC_000012.11:g.72414651del , CM000674.1:g.72414651del GRCh37
NC_000012.10:g.70700918del NCBI36
NG_008279.1:g.87026del

Transcript Alleles

HGVS Amino-acid change
ENST00000333850.4:c.1069-1528del MANE Select ENSP00000329093.3:n.1069-1528del
ENST00000333850.3:c.1069-1528del ENSP00000329093.3:n.1069-1528del
NM_173353.3:c.1069-1528del NP_775489.2:n.1069-1528del
XM_011537899.1:c.475-1528del XP_011536201.1:n.475-1528del
NM_173353.4:c.1069-1528del MANE Select NP_775489.2:n.1069-1528del