Canonical Allele Identifier: CA1948012485
Gene: TH HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.2172047_2172048delinsAG , CM000673.2:g.2172047_2172048delinsAG GRCh38
NC_000011.9:g.2193277_2193278delinsAG , CM000673.1:g.2193277_2193278delinsAG GRCh37
NC_000011.8:g.2149853_2149854delinsAG NCBI36
NG_008128.1:g.4758_4759delinsCT

Transcript Alleles

HGVS Amino-acid Change
XM_011520335.1:c.-262_-261delinsCT XP_011518637.1:n.-262_-261delinsCT
XM_011520335.2:c.-262_-261delinsCT XP_011518637.1:n.-262_-261delinsCT
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