Canonical Allele Identifier: CA15738207

Gene: TPH2

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.71958763T>C , CM000674.2:g.71958763T>C	GRCh38
NC_000012.11:g.72352543T>C , CM000674.1:g.72352543T>C	GRCh37
NC_000012.10:g.70638810T>C	NCBI36
NG_008279.1:g.24918T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333850.4:c.608+9108T>C MANE Select	ENSP00000329093.3:n.608+9108T>C
ENST00000333850.3:c.608+9108T>C	ENSP00000329093.3:n.608+9108T>C
ENST00000546576.1:n.619-2790T>C
NM_173353.3:c.608+9108T>C	NP_775489.2:n.608+9108T>C
XM_011537899.1:c.14+9108T>C	XP_011536201.1:n.14+9108T>C
XR_245894.2:n.709-2790T>C
XR_001748575.1:n.709-2790T>C
NM_173353.4:c.608+9108T>C MANE Select	NP_775489.2:n.608+9108T>C