Canonical Allele Identifier: CA2045506764
Gene: TPH2 HGNC NCBI

Linked Data

dbSNP Id: rs1870976480

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.71938979C>G , CM000674.2:g.71938979C>G GRCh38
NC_000012.11:g.72332759C>G , CM000674.1:g.72332759C>G GRCh37
NC_000012.10:g.70619026C>G NCBI36
NG_008279.1:g.5134C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000333850.4:c.-8C>G MANE Select ENSP00000329093.3:n.-8C>G
ENST00000333850.3:c.-8C>G ENSP00000329093.3:n.-8C>G
ENST00000546576.1:n.3C>G
NM_173353.3:c.-8C>G NP_775489.2:n.-8C>G
XR_245894.2:n.93C>G
XR_001748575.1:n.93C>G
NM_173353.4:c.-8C>G MANE Select NP_775489.2:n.-8C>G