Canonical Allele Identifier: CA2045551465
Gene: TPH2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.72011362A= , CM000674.2:g.72011362A= GRCh38
NC_000012.11:g.72405142A= , CM000674.1:g.72405142A= GRCh37
NC_000012.10:g.70691409A= NCBI36
NG_008279.1:g.77517A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000333850.4:c.1069-11037A= MANE Select ENSP00000329093.3:n.1069-11037A=
ENST00000333850.3:c.1069-11037A= ENSP00000329093.3:n.1069-11037A=
NM_173353.3:c.1069-11037A= NP_775489.2:n.1069-11037A=
XM_011537899.1:c.475-11037A= XP_011536201.1:n.475-11037A=
NM_173353.4:c.1069-11037A= MANE Select NP_775489.2:n.1069-11037A=