Canonical Allele Identifier: CA2619868003
Gene: TPH2 HGNC NCBI

Linked Data

gnomAD v4: 12-71994435-T-G
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.71994435T>G , CM000674.2:g.71994435T>G GRCh38
NC_000012.11:g.72388215T>G , CM000674.1:g.72388215T>G GRCh37
NC_000012.10:g.70674482T>G NCBI36
NG_008279.1:g.60590T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000333850.4:c.942-4T>G MANE Select ENSP00000329093.3:n.942-4T>G
ENST00000333850.3:c.942-4T>G ENSP00000329093.3:n.942-4T>G
NM_173353.3:c.942-4T>G NP_775489.2:n.942-4T>G
XM_011537899.1:c.348-4T>G XP_011536201.1:n.348-4T>G
NM_173353.4:c.942-4T>G MANE Select NP_775489.2:n.942-4T>G
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