Canonical Allele Identifier: CA2045506657
Gene: TPH2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.71938938G= , CM000674.2:g.71938938G= GRCh38
NC_000012.11:g.72332718G= , CM000674.1:g.72332718G= GRCh37
NC_000012.10:g.70618985G= NCBI36
NG_008279.1:g.5093G=

Transcript Alleles

HGVS Amino-acid change
ENST00000333850.4:c.-49G= MANE Select ENSP00000329093.3:n.-49G=
ENST00000333850.3:c.-49G= ENSP00000329093.3:n.-49G=
NM_173353.3:c.-49G= NP_775489.2:n.-49G=
XR_245894.2:n.52G=
XR_001748575.1:n.52G=
NM_173353.4:c.-49G= MANE Select NP_775489.2:n.-49G=