Canonical Allele Identifier: CA1955404360
Gene: TPH1 HGNC NCBI

Linked Data

dbSNP Id: rs915158341
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.18018995T>C , CM000673.2:g.18018995T>C GRCh38
NC_000011.9:g.18040542T>C , CM000673.1:g.18040542T>C GRCh37
NC_000011.8:g.17997118T>C NCBI36
NG_011947.1:g.26794A>G
NG_011947.2:g.26794A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000682019.1:c.*1996A>G MANE Select ENSP00000508368.1:n.*1996A>G
ENST00000250018.6:c.*1996A>G ENSP00000250018.2:n.*1996A>G
NM_004179.3:c.*1996A>G MANE Select NP_004170.1:n.*1996A>G
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