Canonical Allele Identifier: CA2045510549
Gene: TPH2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.71942626T= , CM000674.2:g.71942626T= GRCh38
NC_000012.11:g.72336406T= , CM000674.1:g.72336406T= GRCh37
NC_000012.10:g.70622673T= NCBI36
NG_008279.1:g.8781T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000333850.4:c.255+893T= MANE Select ENSP00000329093.3:n.255+893T=
ENST00000333850.3:c.255+893T= ENSP00000329093.3:n.255+893T=
ENST00000546576.1:n.265+893T=
NM_173353.3:c.255+893T= NP_775489.2:n.255+893T=
XR_245894.2:n.355+893T=
XR_001748575.1:n.355+893T=
NM_173353.4:c.255+893T= MANE Select NP_775489.2:n.255+893T=