Canonical Allele Identifier: CA2045506545
Gene: TPH2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.71938874C= , CM000674.2:g.71938874C= GRCh38
NC_000012.11:g.72332654C= , CM000674.1:g.72332654C= GRCh37
NC_000012.10:g.70618921C= NCBI36
NG_008279.1:g.5029C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000333850.4:c.-113C= MANE Select ENSP00000329093.3:n.-113C=
ENST00000333850.3:c.-113C= ENSP00000329093.3:n.-113C=
NM_173353.3:c.-113C= NP_775489.2:n.-113C=
NM_173353.4:c.-113C= MANE Select NP_775489.2:n.-113C=