Canonical Allele Identifier: CA949088550
Gene: TPH2 HGNC NCBI

Linked Data

dbSNP Id: rs1872652278
gnomAD v3: 12-71994642-T-A
gnomAD v4: 12-71994642-T-A
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.71994642T>A , CM000674.2:g.71994642T>A GRCh38
NC_000012.11:g.72388422T>A , CM000674.1:g.72388422T>A GRCh37
NC_000012.10:g.70674689T>A NCBI36
NG_008279.1:g.60797T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000333850.4:c.1068+77T>A MANE Select ENSP00000329093.3:n.1068+77T>A
ENST00000333850.3:c.1068+77T>A ENSP00000329093.3:n.1068+77T>A
NM_173353.3:c.1068+77T>A NP_775489.2:n.1068+77T>A
XM_011537899.1:c.474+77T>A XP_011536201.1:n.474+77T>A
NM_173353.4:c.1068+77T>A MANE Select NP_775489.2:n.1068+77T>A
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