Canonical Allele Identifier: CA2045551371
Gene: TPH2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.72011277A= , CM000674.2:g.72011277A= GRCh38
NC_000012.11:g.72405057A= , CM000674.1:g.72405057A= GRCh37
NC_000012.10:g.70691324A= NCBI36
NG_008279.1:g.77432A=

Transcript Alleles

HGVS Amino-acid change
ENST00000333850.4:c.1069-11122A= MANE Select ENSP00000329093.3:n.1069-11122A=
ENST00000333850.3:c.1069-11122A= ENSP00000329093.3:n.1069-11122A=
NM_173353.3:c.1069-11122A= NP_775489.2:n.1069-11122A=
XM_011537899.1:c.475-11122A= XP_011536201.1:n.475-11122A=
NM_173353.4:c.1069-11122A= MANE Select NP_775489.2:n.1069-11122A=
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