Canonical Allele Identifier: CA2045506763
Gene: TPH2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.71938979C= , CM000674.2:g.71938979C= GRCh38
NC_000012.11:g.72332759C= , CM000674.1:g.72332759C= GRCh37
NC_000012.10:g.70619026C= NCBI36
NG_008279.1:g.5134C=

Transcript Alleles

HGVS Amino-acid change
ENST00000333850.4:c.-8C= MANE Select ENSP00000329093.3:n.-8C=
ENST00000333850.3:c.-8C= ENSP00000329093.3:n.-8C=
ENST00000546576.1:n.3C=
NM_173353.3:c.-8C= NP_775489.2:n.-8C=
XR_245894.2:n.93C=
XR_001748575.1:n.93C=
NM_173353.4:c.-8C= MANE Select NP_775489.2:n.-8C=