Canonical Allele Identifier: CA2045510578
Gene: TPH2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.71942662A= , CM000674.2:g.71942662A= GRCh38
NC_000012.11:g.72336442A= , CM000674.1:g.72336442A= GRCh37
NC_000012.10:g.70622709A= NCBI36
NG_008279.1:g.8817A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000333850.4:c.255+929A= MANE Select ENSP00000329093.3:n.255+929A=
ENST00000333850.3:c.255+929A= ENSP00000329093.3:n.255+929A=
ENST00000546576.1:n.265+929A=
NM_173353.3:c.255+929A= NP_775489.2:n.255+929A=
XR_245894.2:n.355+929A=
XR_001748575.1:n.355+929A=
NM_173353.4:c.255+929A= MANE Select NP_775489.2:n.255+929A=