Canonical Allele Identifier: CA385782113
Gene: TPH2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr12:g.72388305C>T (hg19) chr12:g.71994525C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.71994525C>T , CM000674.2:g.71994525C>T GRCh38
NC_000012.11:g.72388305C>T , CM000674.1:g.72388305C>T GRCh37
NC_000012.10:g.70674572C>T NCBI36
NG_008279.1:g.60680C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000333850.4:c.1028C>T MANE Select ENSP00000329093.3:p.Ser343Phe
ENST00000333850.3:c.1028C>T ENSP00000329093.3:p.Ser343Phe
NM_173353.3:c.1028C>T NP_775489.2:p.Ser343Phe
XM_011537899.1:c.434C>T XP_011536201.1:p.Ser145Phe
NM_173353.4:c.1028C>T MANE Select NP_775489.2:p.Ser343Phe
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