Canonical Allele Identifier: CA2619867980
Gene: TPH2 HGNC NCBI

Linked Data

gnomAD v4: 12-71994404-T-A
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.71994404T>A , CM000674.2:g.71994404T>A GRCh38
NC_000012.11:g.72388184T>A , CM000674.1:g.72388184T>A GRCh37
NC_000012.10:g.70674451T>A NCBI36
NG_008279.1:g.60559T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000333850.4:c.942-35T>A MANE Select ENSP00000329093.3:n.942-35T>A
ENST00000333850.3:c.942-35T>A ENSP00000329093.3:n.942-35T>A
NM_173353.3:c.942-35T>A NP_775489.2:n.942-35T>A
XM_011537899.1:c.348-35T>A XP_011536201.1:n.348-35T>A
NM_173353.4:c.942-35T>A MANE Select NP_775489.2:n.942-35T>A
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