Canonical Allele Identifier: CA239239805
Gene: TPH2 HGNC NCBI

Linked Data

dbSNP Id: rs569229705
gnomAD v2: 12-72414722-C-CA
gnomAD v3: 12-72020942-C-CA
gnomAD v4: 12-72020942-C-CA
MyVariant Identifiers: chr12:g.72414722_72414723insA (hg19) chr12:g.72020942_72020943insA (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.72020949dup , CM000674.2:g.72020949dup GRCh38
NC_000012.11:g.72414729dup , CM000674.1:g.72414729dup GRCh37
NC_000012.10:g.70700996dup NCBI36
NG_008279.1:g.87104dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000333850.4:c.1069-1450dup MANE Select ENSP00000329093.3:n.1069-1450dup
ENST00000333850.3:c.1069-1450dup ENSP00000329093.3:n.1069-1450dup
NM_173353.3:c.1069-1450dup NP_775489.2:n.1069-1450dup
XM_011537899.1:c.475-1450dup XP_011536201.1:n.475-1450dup
NM_173353.4:c.1069-1450dup MANE Select NP_775489.2:n.1069-1450dup
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