Canonical Allele Identifier: CA691603067
Gene: TPH2 HGNC NCBI

Linked Data

dbSNP Id: rs1190748592
gnomAD v3: 12-72018778-A-G
gnomAD v4: 12-72018778-A-G
MyVariant Identifiers: chr12:g.72412558A>G (hg19) chr12:g.72018778A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.72018778A>G , CM000674.2:g.72018778A>G GRCh38
NC_000012.11:g.72412558A>G , CM000674.1:g.72412558A>G GRCh37
NC_000012.10:g.70698825A>G NCBI36
NG_008279.1:g.84933A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000333850.4:c.1069-3621A>G MANE Select ENSP00000329093.3:n.1069-3621A>G
ENST00000333850.3:c.1069-3621A>G ENSP00000329093.3:n.1069-3621A>G
NM_173353.3:c.1069-3621A>G NP_775489.2:n.1069-3621A>G
XM_011537899.1:c.475-3621A>G XP_011536201.1:n.475-3621A>G
NM_173353.4:c.1069-3621A>G MANE Select NP_775489.2:n.1069-3621A>G
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