Canonical Allele Identifier: CA2045506665
Gene: TPH2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.71938940C= , CM000674.2:g.71938940C= GRCh38
NC_000012.11:g.72332720C= , CM000674.1:g.72332720C= GRCh37
NC_000012.10:g.70618987C= NCBI36
NG_008279.1:g.5095C=

Transcript Alleles

HGVS Amino-acid change
ENST00000333850.4:c.-47C= MANE Select ENSP00000329093.3:n.-47C=
ENST00000333850.3:c.-47C= ENSP00000329093.3:n.-47C=
NM_173353.3:c.-47C= NP_775489.2:n.-47C=
XR_245894.2:n.54C=
XR_001748575.1:n.54C=
NM_173353.4:c.-47C= MANE Select NP_775489.2:n.-47C=