Canonical Allele Identifier: CA2516014983
Gene: TPH2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.71983570C>G , CM000674.2:g.71983570C>G GRCh38
NC_000012.11:g.72377350C>G , CM000674.1:g.72377350C>G GRCh37
NC_000012.10:g.70663617C>G NCBI36
NG_008279.1:g.49725C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000333850.4:c.941+4483C>G MANE Select ENSP00000329093.3:n.941+4483C>G
ENST00000333850.3:c.941+4483C>G ENSP00000329093.3:n.941+4483C>G
NM_173353.3:c.941+4483C>G NP_775489.2:n.941+4483C>G
XM_011537899.1:c.347+4483C>G XP_011536201.1:n.347+4483C>G
NM_173353.4:c.941+4483C>G MANE Select NP_775489.2:n.941+4483C>G
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