Canonical Allele Identifier: CA6689615
Gene: TPH2 HGNC NCBI

Linked Data

dbSNP Id: rs776929541

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.71938939C>T , CM000674.2:g.71938939C>T GRCh38
NC_000012.11:g.72332719C>T , CM000674.1:g.72332719C>T GRCh37
NC_000012.10:g.70618986C>T NCBI36
NG_008279.1:g.5094C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000333850.4:c.-48C>T MANE Select ENSP00000329093.3:n.-48C>T
ENST00000333850.3:c.-48C>T ENSP00000329093.3:n.-48C>T
NM_173353.3:c.-48C>T NP_775489.2:n.-48C>T
XR_245894.2:n.53C>T
XR_001748575.1:n.53C>T
NM_173353.4:c.-48C>T MANE Select NP_775489.2:n.-48C>T