Canonical Allele Identifier: CA2575227517
Gene: TPH2 HGNC NCBI

Linked Data

gnomAD v4: 12-71938928-CGCTGCTACTGCCCCTCTAGTACCCCCT-C
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.71938934_71938960del , CM000674.2:g.71938934_71938960del GRCh38
NC_000012.11:g.72332714_72332740del , CM000674.1:g.72332714_72332740del GRCh37
NC_000012.10:g.70618981_70619007del NCBI36
NG_008279.1:g.5089_5115del

Transcript Alleles

HGVS Amino-acid change
ENST00000333850.4:c.-53_-27del MANE Select ENSP00000329093.3:n.-53_-27del
ENST00000333850.3:c.-53_-27del ENSP00000329093.3:n.-53_-27del
NM_173353.3:c.-53_-27del NP_775489.2:n.-53_-27del
XR_245894.2:n.48_74del
XR_001748575.1:n.48_74del
NM_173353.4:c.-53_-27del MANE Select NP_775489.2:n.-53_-27del
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