Canonical Allele Identifier: CA2045528207
Gene: TPH2 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.71983559T= , CM000674.2:g.71983559T= GRCh38
NC_000012.11:g.72377339T= , CM000674.1:g.72377339T= GRCh37
NC_000012.10:g.70663606T= NCBI36
NG_008279.1:g.49714T=

Transcript Alleles

HGVS Amino-acid change
ENST00000333850.4:c.941+4472T= MANE Select ENSP00000329093.3:n.941+4472T=
ENST00000333850.3:c.941+4472T= ENSP00000329093.3:n.941+4472T=
NM_173353.3:c.941+4472T= NP_775489.2:n.941+4472T=
XM_011537899.1:c.347+4472T= XP_011536201.1:n.347+4472T=
NM_173353.4:c.941+4472T= MANE Select NP_775489.2:n.941+4472T=
Search 100 bp 5'
Search 100 bp 3'