Canonical Allele Identifier: CA1955404355
Gene: TPH1 HGNC NCBI

Linked Data

dbSNP Id: rs1854328171

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.18018981T>C , CM000673.2:g.18018981T>C GRCh38
NC_000011.9:g.18040528T>C , CM000673.1:g.18040528T>C GRCh37
NC_000011.8:g.17997104T>C NCBI36
NG_011947.1:g.26808A>G
NG_011947.2:g.26808A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000682019.1:c.*2010A>G MANE Select ENSP00000508368.1:n.*2010A>G
ENST00000250018.6:c.*2010A>G ENSP00000250018.2:n.*2010A>G
NM_004179.3:c.*2010A>G MANE Select NP_004170.1:n.*2010A>G