Canonical Allele Identifier: CA2612710795
Gene: TPH1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.18019070A>C , CM000673.2:g.18019070A>C GRCh38
NC_000011.9:g.18040617A>C , CM000673.1:g.18040617A>C GRCh37
NC_000011.8:g.17997193A>C NCBI36
NG_011947.1:g.26719T>G
NG_011947.2:g.26719T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000682019.1:c.*1921T>G MANE Select ENSP00000508368.1:n.*1921T>G
ENST00000250018.6:c.*1921T>G ENSP00000250018.2:n.*1921T>G
NM_004179.3:c.*1921T>G MANE Select NP_004170.1:n.*1921T>G