Canonical Allele Identifier: CA2045564488
Gene: TPH2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.72020677G= , CM000674.2:g.72020677G= GRCh38
NC_000012.11:g.72414457G= , CM000674.1:g.72414457G= GRCh37
NC_000012.10:g.70700724G= NCBI36
NG_008279.1:g.86832G=

Transcript Alleles

HGVS Amino-acid change
ENST00000333850.4:c.1069-1722G= MANE Select ENSP00000329093.3:n.1069-1722G=
ENST00000333850.3:c.1069-1722G= ENSP00000329093.3:n.1069-1722G=
NM_173353.3:c.1069-1722G= NP_775489.2:n.1069-1722G=
XM_011537899.1:c.475-1722G= XP_011536201.1:n.475-1722G=
NM_173353.4:c.1069-1722G= MANE Select NP_775489.2:n.1069-1722G=