Canonical Allele Identifier: CA691585442
Gene: TPH2 HGNC NCBI

Linked Data

dbSNP Id: rs1243151503
MyVariant Identifiers: chr12:g.72377344G>A (hg19) chr12:g.71983564G>A (hg38)
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Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid change
ENST00000333850.4:c.941+4477G>A MANE Select ENSP00000329093.3:n.941+4477G>A
ENST00000333850.3:c.941+4477G>A ENSP00000329093.3:n.941+4477G>A
NM_173353.3:c.941+4477G>A NP_775489.2:n.941+4477G>A
XM_011537899.1:c.347+4477G>A XP_011536201.1:n.347+4477G>A
NM_173353.4:c.941+4477G>A MANE Select NP_775489.2:n.941+4477G>A
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