Canonical Allele Identifier: CA239239654
Gene: TPH2 HGNC NCBI

Linked Data

dbSNP Id: rs957041566

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.72020825G>C , CM000674.2:g.72020825G>C GRCh38
NC_000012.11:g.72414605G>C , CM000674.1:g.72414605G>C GRCh37
NC_000012.10:g.70700872G>C NCBI36
NG_008279.1:g.86980G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000333850.4:c.1069-1574G>C MANE Select ENSP00000329093.3:n.1069-1574G>C
ENST00000333850.3:c.1069-1574G>C ENSP00000329093.3:n.1069-1574G>C
NM_173353.3:c.1069-1574G>C NP_775489.2:n.1069-1574G>C
XM_011537899.1:c.475-1574G>C XP_011536201.1:n.475-1574G>C
NM_173353.4:c.1069-1574G>C MANE Select NP_775489.2:n.1069-1574G>C