Canonical Allele Identifier: CA239219021
Gene: TPH2 HGNC NCBI

Linked Data

dbSNP Id: rs774463883
MyVariant Identifiers: chr12:g.72377151_72377152insA (hg19) chr12:g.71983371_71983372insA (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.71983374dup , CM000674.2:g.71983374dup GRCh38
NC_000012.11:g.72377154dup , CM000674.1:g.72377154dup GRCh37
NC_000012.10:g.70663421dup NCBI36
NG_008279.1:g.49529dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000333850.4:c.941+4287dup MANE Select ENSP00000329093.3:n.941+4287dup
ENST00000333850.3:c.941+4287dup ENSP00000329093.3:n.941+4287dup
NM_173353.3:c.941+4287dup NP_775489.2:n.941+4287dup
XM_011537899.1:c.347+4287dup XP_011536201.1:n.347+4287dup
NM_173353.4:c.941+4287dup MANE Select NP_775489.2:n.941+4287dup
Search 100 bp 5'
Search 100 bp 3'