Canonical Allele Identifier: CA385782044
Gene: TPH2 HGNC NCBI

Linked Data

gnomAD v4: 12-71994512-A-G
MyVariant Identifiers: chr12:g.72388292A>G (hg19) chr12:g.71994512A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.71994512A>G , CM000674.2:g.71994512A>G GRCh38
NC_000012.11:g.72388292A>G , CM000674.1:g.72388292A>G GRCh37
NC_000012.10:g.70674559A>G NCBI36
NG_008279.1:g.60667A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000333850.4:c.1015A>G MANE Select ENSP00000329093.3:p.Ile339Val
ENST00000333850.3:c.1015A>G ENSP00000329093.3:p.Ile339Val
NM_173353.3:c.1015A>G NP_775489.2:p.Ile339Val
XM_011537899.1:c.421A>G XP_011536201.1:p.Ile141Val
NM_173353.4:c.1015A>G MANE Select NP_775489.2:p.Ile339Val
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