Canonical Allele Identifier: CA2045533056
Gene: TPH2 HGNC NCBI

Linked Data

dbSNP Id: rs1566148580
gnomAD v4: 12-71994427-C-T
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.71994427C>T , CM000674.2:g.71994427C>T GRCh38
NC_000012.11:g.72388207C>T , CM000674.1:g.72388207C>T GRCh37
NC_000012.10:g.70674474C>T NCBI36
NG_008279.1:g.60582C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000333850.4:c.942-12C>T MANE Select ENSP00000329093.3:n.942-12C>T
ENST00000333850.3:c.942-12C>T ENSP00000329093.3:n.942-12C>T
NM_173353.3:c.942-12C>T NP_775489.2:n.942-12C>T
XM_011537899.1:c.348-12C>T XP_011536201.1:n.348-12C>T
NM_173353.4:c.942-12C>T MANE Select NP_775489.2:n.942-12C>T
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