Canonical Allele Identifier: CA218519041
Gene: TPH1 HGNC NCBI

Linked Data

dbSNP Id: rs59097435
MyVariant Identifiers: chr11:g.18040512G>A (hg19) chr11:g.18018965G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.18018965G>A , CM000673.2:g.18018965G>A GRCh38
NC_000011.9:g.18040512G>A , CM000673.1:g.18040512G>A GRCh37
NC_000011.8:g.17997088G>A NCBI36
NG_011947.1:g.26824C>T
NG_011947.2:g.26824C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000682019.1:c.*2026C>T MANE Select ENSP00000508368.1:n.*2026C>T
ENST00000250018.6:c.*2026C>T ENSP00000250018.2:n.*2026C>T
NM_004179.3:c.*2026C>T MANE Select NP_004170.1:n.*2026C>T
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