Canonical Allele Identifier: CA2045533151
Gene: TPH2 HGNC NCBI

Linked Data

dbSNP Id: rs1872652326
gnomAD v4: 12-71994643-A-G
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.71994643A>G , CM000674.2:g.71994643A>G GRCh38
NC_000012.11:g.72388423A>G , CM000674.1:g.72388423A>G GRCh37
NC_000012.10:g.70674690A>G NCBI36
NG_008279.1:g.60798A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000333850.4:c.1068+78A>G MANE Select ENSP00000329093.3:n.1068+78A>G
ENST00000333850.3:c.1068+78A>G ENSP00000329093.3:n.1068+78A>G
NM_173353.3:c.1068+78A>G NP_775489.2:n.1068+78A>G
XM_011537899.1:c.474+78A>G XP_011536201.1:n.474+78A>G
NM_173353.4:c.1068+78A>G MANE Select NP_775489.2:n.1068+78A>G
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