Canonical Allele Identifier: CA2045506717
Gene: TPH2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.71938958T= , CM000674.2:g.71938958T= GRCh38
NC_000012.11:g.72332738T= , CM000674.1:g.72332738T= GRCh37
NC_000012.10:g.70619005T= NCBI36
NG_008279.1:g.5113T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000333850.4:c.-29T= MANE Select ENSP00000329093.3:n.-29T=
ENST00000333850.3:c.-29T= ENSP00000329093.3:n.-29T=
NM_173353.3:c.-29T= NP_775489.2:n.-29T=
XR_245894.2:n.72T=
XR_001748575.1:n.72T=
NM_173353.4:c.-29T= MANE Select NP_775489.2:n.-29T=