Canonical Allele Identifier: CA2726686513
Gene: TPH2 HGNC NCBI

Linked Data

dbSNP Id: rs2139173444

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.71938945del , CM000674.2:g.71938945del GRCh38
NC_000012.11:g.72332725del , CM000674.1:g.72332725del GRCh37
NC_000012.10:g.70618992del NCBI36
NG_008279.1:g.5100del

Transcript Alleles

HGVS Amino-acid change
ENST00000333850.4:c.-42del MANE Select ENSP00000329093.3:n.-42del
ENST00000333850.3:c.-42del ENSP00000329093.3:n.-42del
NM_173353.3:c.-42del NP_775489.2:n.-42del
XR_245894.2:n.59del
XR_001748575.1:n.59del
NM_173353.4:c.-42del MANE Select NP_775489.2:n.-42del