Canonical Allele Identifier: CA2045528211
Gene: TPH2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.71983569T= , CM000674.2:g.71983569T= GRCh38
NC_000012.11:g.72377349T= , CM000674.1:g.72377349T= GRCh37
NC_000012.10:g.70663616T= NCBI36
NG_008279.1:g.49724T=

Transcript Alleles

HGVS Amino-acid change
ENST00000333850.4:c.941+4482T= MANE Select ENSP00000329093.3:n.941+4482T=
ENST00000333850.3:c.941+4482T= ENSP00000329093.3:n.941+4482T=
NM_173353.3:c.941+4482T= NP_775489.2:n.941+4482T=
XM_011537899.1:c.347+4482T= XP_011536201.1:n.347+4482T=
NM_173353.4:c.941+4482T= MANE Select NP_775489.2:n.941+4482T=
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