Canonical Allele Identifier: CA2045510994
Gene: TPH2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.71943081A= , CM000674.2:g.71943081A= GRCh38
NC_000012.11:g.72336861A= , CM000674.1:g.72336861A= GRCh37
NC_000012.10:g.70623128A= NCBI36
NG_008279.1:g.9236A=

Transcript Alleles

HGVS Amino-acid change
ENST00000333850.4:c.256-1213A= MANE Select ENSP00000329093.3:n.256-1213A=
ENST00000333850.3:c.256-1213A= ENSP00000329093.3:n.256-1213A=
ENST00000546576.1:n.266-1213A=
NM_173353.3:c.256-1213A= NP_775489.2:n.256-1213A=
XR_245894.2:n.356-1213A=
XR_001748575.1:n.356-1213A=
NM_173353.4:c.256-1213A= MANE Select NP_775489.2:n.256-1213A=