Canonical Allele Identifier: CA2045510952
Gene: TPH2 HGNC NCBI

Linked Data

dbSNP Id: rs1871116121
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.71943052del , CM000674.2:g.71943052del GRCh38
NC_000012.11:g.72336832del , CM000674.1:g.72336832del GRCh37
NC_000012.10:g.70623099del NCBI36
NG_008279.1:g.9207del

Transcript Alleles

HGVS Amino-acid change
ENST00000333850.4:c.256-1242del MANE Select ENSP00000329093.3:n.256-1242del
ENST00000333850.3:c.256-1242del ENSP00000329093.3:n.256-1242del
ENST00000546576.1:n.266-1242del
NM_173353.3:c.256-1242del NP_775489.2:n.256-1242del
XR_245894.2:n.356-1242del
XR_001748575.1:n.356-1242del
NM_173353.4:c.256-1242del MANE Select NP_775489.2:n.256-1242del
Search 100 bp 5'
Search 100 bp 3'