Canonical Allele Identifier: CA2612710805
Gene: TPH1 HGNC NCBI

Linked Data

gnomAD v4: 11-18019101-C-A
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.18019101C>A , CM000673.2:g.18019101C>A GRCh38
NC_000011.9:g.18040648C>A , CM000673.1:g.18040648C>A GRCh37
NC_000011.8:g.17997224C>A NCBI36
NG_011947.1:g.26688G>T
NG_011947.2:g.26688G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000682019.1:c.*1890G>T MANE Select ENSP00000508368.1:n.*1890G>T
ENST00000250018.6:c.*1890G>T ENSP00000250018.2:n.*1890G>T
NM_004179.3:c.*1890G>T MANE Select NP_004170.1:n.*1890G>T
Search 100 bp 5'
Search 100 bp 3'