Canonical Allele Identifier: CA691599062
Gene: TPH2 HGNC NCBI

Linked Data

dbSNP Id: rs1445217237
MyVariant Identifiers: chr12:g.72404486A>C (hg19) chr12:g.72010706A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.72010706A>C , CM000674.2:g.72010706A>C GRCh38
NC_000012.11:g.72404486A>C , CM000674.1:g.72404486A>C GRCh37
NC_000012.10:g.70690753A>C NCBI36
NG_008279.1:g.76861A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000333850.4:c.1069-11693A>C MANE Select ENSP00000329093.3:n.1069-11693A>C
ENST00000333850.3:c.1069-11693A>C ENSP00000329093.3:n.1069-11693A>C
NM_173353.3:c.1069-11693A>C NP_775489.2:n.1069-11693A>C
XM_011537899.1:c.475-11693A>C XP_011536201.1:n.475-11693A>C
NM_173353.4:c.1069-11693A>C MANE Select NP_775489.2:n.1069-11693A>C
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