Canonical Allele Identifier: CA2045550698
Gene: TPH2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.72010781T= , CM000674.2:g.72010781T= GRCh38
NC_000012.11:g.72404561T= , CM000674.1:g.72404561T= GRCh37
NC_000012.10:g.70690828T= NCBI36
NG_008279.1:g.76936T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000333850.4:c.1069-11618T= MANE Select ENSP00000329093.3:n.1069-11618T=
ENST00000333850.3:c.1069-11618T= ENSP00000329093.3:n.1069-11618T=
NM_173353.3:c.1069-11618T= NP_775489.2:n.1069-11618T=
XM_011537899.1:c.475-11618T= XP_011536201.1:n.475-11618T=
NM_173353.4:c.1069-11618T= MANE Select NP_775489.2:n.1069-11618T=