Canonical Allele Identifier: CA949091169

Gene: TPH2

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.71948504C>A , CM000674.2:g.71948504C>A	GRCh38
NC_000012.11:g.72342284C>A , CM000674.1:g.72342284C>A	GRCh37
NC_000012.10:g.70628551C>A	NCBI36
NG_008279.1:g.14659C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333850.4:c.541-1084C>A MANE Select	ENSP00000329093.3:n.541-1084C>A
ENST00000333850.3:c.541-1084C>A	ENSP00000329093.3:n.541-1084C>A
ENST00000546576.1:n.551-1084C>A
NM_173353.3:c.541-1084C>A	NP_775489.2:n.541-1084C>A
XM_011537899.1:c.-55+500C>A	XP_011536201.1:n.-55+500C>A
XR_245894.2:n.641-1084C>A
XR_001748575.1:n.641-1084C>A
NM_173353.4:c.541-1084C>A MANE Select	NP_775489.2:n.541-1084C>A