Canonical Allele Identifier: CA2045564637
Gene: TPH2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.72020744C= , CM000674.2:g.72020744C= GRCh38
NC_000012.11:g.72414524C= , CM000674.1:g.72414524C= GRCh37
NC_000012.10:g.70700791C= NCBI36
NG_008279.1:g.86899C=

Transcript Alleles

HGVS Amino-acid change
ENST00000333850.4:c.1069-1655C= MANE Select ENSP00000329093.3:n.1069-1655C=
ENST00000333850.3:c.1069-1655C= ENSP00000329093.3:n.1069-1655C=
NM_173353.3:c.1069-1655C= NP_775489.2:n.1069-1655C=
XM_011537899.1:c.475-1655C= XP_011536201.1:n.475-1655C=
NM_173353.4:c.1069-1655C= MANE Select NP_775489.2:n.1069-1655C=