Canonical Allele Identifier: CA605812780
Gene: TPH2 HGNC NCBI

Linked Data

dbSNP Id: rs1487909264
gnomAD v2: 12-72414389-C-T
gnomAD v3: 12-72020609-C-T
gnomAD v4: 12-72020609-C-T
MyVariant Identifiers: chr12:g.72414389C>T (hg19) chr12:g.72020609C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.72020609C>T , CM000674.2:g.72020609C>T GRCh38
NC_000012.11:g.72414389C>T , CM000674.1:g.72414389C>T GRCh37
NC_000012.10:g.70700656C>T NCBI36
NG_008279.1:g.86764C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000333850.4:c.1069-1790C>T MANE Select ENSP00000329093.3:n.1069-1790C>T
ENST00000333850.3:c.1069-1790C>T ENSP00000329093.3:n.1069-1790C>T
NM_173353.3:c.1069-1790C>T NP_775489.2:n.1069-1790C>T
XM_011537899.1:c.475-1790C>T XP_011536201.1:n.475-1790C>T
NM_173353.4:c.1069-1790C>T MANE Select NP_775489.2:n.1069-1790C>T
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