Canonical Allele Identifier: CA2612710798
Gene: TPH1 HGNC NCBI

Linked Data

gnomAD v4: 11-18019072-C-T
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.18019072C>T , CM000673.2:g.18019072C>T GRCh38
NC_000011.9:g.18040619C>T , CM000673.1:g.18040619C>T GRCh37
NC_000011.8:g.17997195C>T NCBI36
NG_011947.1:g.26717G>A
NG_011947.2:g.26717G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000682019.1:c.*1919G>A MANE Select ENSP00000508368.1:n.*1919G>A
ENST00000250018.6:c.*1919G>A ENSP00000250018.2:n.*1919G>A
NM_004179.3:c.*1919G>A MANE Select NP_004170.1:n.*1919G>A
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