Canonical Allele Identifier: CA1955404341
Gene: TPH1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.18018952C= , CM000673.2:g.18018952C= GRCh38
NC_000011.9:g.18040499C= , CM000673.1:g.18040499C= GRCh37
NC_000011.8:g.17997075C= NCBI36
NG_011947.1:g.26837G=
NG_011947.2:g.26837G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000682019.1:c.*2039G= MANE Select ENSP00000508368.1:n.*2039G=
ENST00000250018.6:c.*2039G= ENSP00000250018.2:n.*2039G=
NM_004179.3:c.*2039G= MANE Select NP_004170.1:n.*2039G=
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