Canonical Allele Identifier: CA949084651
Gene: TPH2 HGNC NCBI

Linked Data

gnomAD v3: 12-71983564-G-T
gnomAD v4: 12-71983564-G-T
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.71983564G>T , CM000674.2:g.71983564G>T GRCh38
NC_000012.11:g.72377344G>T , CM000674.1:g.72377344G>T GRCh37
NC_000012.10:g.70663611G>T NCBI36
NG_008279.1:g.49719G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000333850.4:c.941+4477G>T MANE Select ENSP00000329093.3:n.941+4477G>T
ENST00000333850.3:c.941+4477G>T ENSP00000329093.3:n.941+4477G>T
NM_173353.3:c.941+4477G>T NP_775489.2:n.941+4477G>T
XM_011537899.1:c.347+4477G>T XP_011536201.1:n.347+4477G>T
NM_173353.4:c.941+4477G>T MANE Select NP_775489.2:n.941+4477G>T
Search 100 bp 5'
Search 100 bp 3'