Canonical Allele Identifier: CA2619868078
Gene: TPH2 HGNC NCBI

Linked Data

gnomAD v4: 12-71994628-TC-T
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.71994629del , CM000674.2:g.71994629del GRCh38
NC_000012.11:g.72388409del , CM000674.1:g.72388409del GRCh37
NC_000012.10:g.70674676del NCBI36
NG_008279.1:g.60784del

Transcript Alleles

HGVS Amino-acid change
ENST00000333850.4:c.1068+64del MANE Select ENSP00000329093.3:n.1068+64del
ENST00000333850.3:c.1068+64del ENSP00000329093.3:n.1068+64del
NM_173353.3:c.1068+64del NP_775489.2:n.1068+64del
XM_011537899.1:c.474+64del XP_011536201.1:n.474+64del
NM_173353.4:c.1068+64del MANE Select NP_775489.2:n.1068+64del
Search 100 bp 5'
Search 100 bp 3'