Canonical Allele Identifier: CA2612710793
Gene: TPH1 HGNC NCBI

Linked Data

gnomAD v4: 11-18019063-T-C
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.18019063T>C , CM000673.2:g.18019063T>C GRCh38
NC_000011.9:g.18040610T>C , CM000673.1:g.18040610T>C GRCh37
NC_000011.8:g.17997186T>C NCBI36
NG_011947.1:g.26726A>G
NG_011947.2:g.26726A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000682019.1:c.*1928A>G MANE Select ENSP00000508368.1:n.*1928A>G
ENST00000250018.6:c.*1928A>G ENSP00000250018.2:n.*1928A>G
NM_004179.3:c.*1928A>G MANE Select NP_004170.1:n.*1928A>G
Search 100 bp 5'
Search 100 bp 3'