Canonical Allele Identifier: CA385782172
Gene: TPH2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr12:g.72388317C>A (hg19) chr12:g.71994537C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.71994537C>A , CM000674.2:g.71994537C>A GRCh38
NC_000012.11:g.72388317C>A , CM000674.1:g.72388317C>A GRCh37
NC_000012.10:g.70674584C>A NCBI36
NG_008279.1:g.60692C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000333850.4:c.1040C>A MANE Select ENSP00000329093.3:p.Ser347Ter
ENST00000333850.3:c.1040C>A ENSP00000329093.3:p.Ser347Ter
NM_173353.3:c.1040C>A NP_775489.2:p.Ser347Ter
XM_011537899.1:c.446C>A XP_011536201.1:p.Ser149Ter
NM_173353.4:c.1040C>A MANE Select NP_775489.2:p.Ser347Ter
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