Canonical Allele Identifier: CA949097316
Gene: TPH2 HGNC NCBI

Linked Data

gnomAD v3: 12-72020647-CA-C
gnomAD v4: 12-72020647-CA-C
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.72020648del , CM000674.2:g.72020648del GRCh38
NC_000012.11:g.72414428del , CM000674.1:g.72414428del GRCh37
NC_000012.10:g.70700695del NCBI36
NG_008279.1:g.86803del

Transcript Alleles

HGVS Amino-acid change
ENST00000333850.4:c.1069-1751del MANE Select ENSP00000329093.3:n.1069-1751del
ENST00000333850.3:c.1069-1751del ENSP00000329093.3:n.1069-1751del
NM_173353.3:c.1069-1751del NP_775489.2:n.1069-1751del
XM_011537899.1:c.475-1751del XP_011536201.1:n.475-1751del
NM_173353.4:c.1069-1751del MANE Select NP_775489.2:n.1069-1751del
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