Canonical Allele Identifier: CA691603932
Gene: TPH2 HGNC NCBI

Linked Data

dbSNP Id: rs986516442

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.72020832A>C , CM000674.2:g.72020832A>C GRCh38
NC_000012.11:g.72414612A>C , CM000674.1:g.72414612A>C GRCh37
NC_000012.10:g.70700879A>C NCBI36
NG_008279.1:g.86987A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000333850.4:c.1069-1567A>C MANE Select ENSP00000329093.3:n.1069-1567A>C
ENST00000333850.3:c.1069-1567A>C ENSP00000329093.3:n.1069-1567A>C
NM_173353.3:c.1069-1567A>C NP_775489.2:n.1069-1567A>C
XM_011537899.1:c.475-1567A>C XP_011536201.1:n.475-1567A>C
NM_173353.4:c.1069-1567A>C MANE Select NP_775489.2:n.1069-1567A>C