Canonical Allele Identifier: CA239239554
Gene: TPH2 HGNC NCBI

Linked Data

dbSNP Id: rs1032144244

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.72020708A>G , CM000674.2:g.72020708A>G GRCh38
NC_000012.11:g.72414488A>G , CM000674.1:g.72414488A>G GRCh37
NC_000012.10:g.70700755A>G NCBI36
NG_008279.1:g.86863A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000333850.4:c.1069-1691A>G MANE Select ENSP00000329093.3:n.1069-1691A>G
ENST00000333850.3:c.1069-1691A>G ENSP00000329093.3:n.1069-1691A>G
NM_173353.3:c.1069-1691A>G NP_775489.2:n.1069-1691A>G
XM_011537899.1:c.475-1691A>G XP_011536201.1:n.475-1691A>G
NM_173353.4:c.1069-1691A>G MANE Select NP_775489.2:n.1069-1691A>G