Canonical Allele Identifier: CA2045551500
Gene: TPH2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.72011419T= , CM000674.2:g.72011419T= GRCh38
NC_000012.11:g.72405199T= , CM000674.1:g.72405199T= GRCh37
NC_000012.10:g.70691466T= NCBI36
NG_008279.1:g.77574T=

Transcript Alleles

HGVS Amino-acid change
ENST00000333850.4:c.1069-10980T= MANE Select ENSP00000329093.3:n.1069-10980T=
ENST00000333850.3:c.1069-10980T= ENSP00000329093.3:n.1069-10980T=
NM_173353.3:c.1069-10980T= NP_775489.2:n.1069-10980T=
XM_011537899.1:c.475-10980T= XP_011536201.1:n.475-10980T=
NM_173353.4:c.1069-10980T= MANE Select NP_775489.2:n.1069-10980T=
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