Canonical Allele Identifier: CA2045506742
Gene: TPH2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.71938978C= , CM000674.2:g.71938978C= GRCh38
NC_000012.11:g.72332758C= , CM000674.1:g.72332758C= GRCh37
NC_000012.10:g.70619025C= NCBI36
NG_008279.1:g.5133C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000333850.4:c.-9C= MANE Select ENSP00000329093.3:n.-9C=
ENST00000333850.3:c.-9C= ENSP00000329093.3:n.-9C=
ENST00000546576.1:n.2C=
NM_173353.3:c.-9C= NP_775489.2:n.-9C=
XR_245894.2:n.92C=
XR_001748575.1:n.92C=
NM_173353.4:c.-9C= MANE Select NP_775489.2:n.-9C=