Canonical Allele Identifier: CA2045506680
Gene: TPH2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.71938949A= , CM000674.2:g.71938949A= GRCh38
NC_000012.11:g.72332729A= , CM000674.1:g.72332729A= GRCh37
NC_000012.10:g.70618996A= NCBI36
NG_008279.1:g.5104A=

Transcript Alleles

HGVS Amino-acid change
ENST00000333850.4:c.-38A= MANE Select ENSP00000329093.3:n.-38A=
ENST00000333850.3:c.-38A= ENSP00000329093.3:n.-38A=
NM_173353.3:c.-38A= NP_775489.2:n.-38A=
XR_245894.2:n.63A=
XR_001748575.1:n.63A=
NM_173353.4:c.-38A= MANE Select NP_775489.2:n.-38A=