Canonical Allele Identifier: CA239232737
Gene: TPH2 HGNC NCBI

Linked Data

dbSNP Id: rs1007061726
MyVariant Identifiers: chr12:g.72404464T>A (hg19) chr12:g.72010684T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.72010684T>A , CM000674.2:g.72010684T>A GRCh38
NC_000012.11:g.72404464T>A , CM000674.1:g.72404464T>A GRCh37
NC_000012.10:g.70690731T>A NCBI36
NG_008279.1:g.76839T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000333850.4:c.1069-11715T>A MANE Select ENSP00000329093.3:n.1069-11715T>A
ENST00000333850.3:c.1069-11715T>A ENSP00000329093.3:n.1069-11715T>A
NM_173353.3:c.1069-11715T>A NP_775489.2:n.1069-11715T>A
XM_011537899.1:c.475-11715T>A XP_011536201.1:n.475-11715T>A
NM_173353.4:c.1069-11715T>A MANE Select NP_775489.2:n.1069-11715T>A
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