Canonical Allele Identifier: CA2619868068
Gene: TPH2 HGNC NCBI

Linked Data

gnomAD v4: 12-71994604-TC-T
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.71994606del , CM000674.2:g.71994606del GRCh38
NC_000012.11:g.72388386del , CM000674.1:g.72388386del GRCh37
NC_000012.10:g.70674653del NCBI36
NG_008279.1:g.60761del

Transcript Alleles

HGVS Amino-acid change
ENST00000333850.4:c.1068+41del MANE Select ENSP00000329093.3:n.1068+41del
ENST00000333850.3:c.1068+41del ENSP00000329093.3:n.1068+41del
NM_173353.3:c.1068+41del NP_775489.2:n.1068+41del
XM_011537899.1:c.474+41del XP_011536201.1:n.474+41del
NM_173353.4:c.1068+41del MANE Select NP_775489.2:n.1068+41del
Search 100 bp 5'
Search 100 bp 3'