Canonical Allele Identifier: CA2045510755
Gene: TPH2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.71942855A= , CM000674.2:g.71942855A= GRCh38
NC_000012.11:g.72336635A= , CM000674.1:g.72336635A= GRCh37
NC_000012.10:g.70622902A= NCBI36
NG_008279.1:g.9010A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000333850.4:c.255+1122A= MANE Select ENSP00000329093.3:n.255+1122A=
ENST00000333850.3:c.255+1122A= ENSP00000329093.3:n.255+1122A=
ENST00000546576.1:n.265+1122A=
NM_173353.3:c.255+1122A= NP_775489.2:n.255+1122A=
XR_245894.2:n.355+1122A=
XR_001748575.1:n.355+1122A=
NM_173353.4:c.255+1122A= MANE Select NP_775489.2:n.255+1122A=