Canonical Allele Identifier: CA1948012540
Gene: TH HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.2172081_2172082delinsAG , CM000673.2:g.2172081_2172082delinsAG GRCh38
NC_000011.9:g.2193311_2193312delinsAG , CM000673.1:g.2193311_2193312delinsAG GRCh37
NC_000011.8:g.2149887_2149888delinsAG NCBI36
NG_008128.1:g.4724_4725delinsCT

Transcript Alleles

HGVS Amino-acid Change
XM_011520335.1:c.-296_-295delinsCT XP_011518637.1:n.-296_-295delinsCT
XM_011520335.2:c.-296_-295delinsCT XP_011518637.1:n.-296_-295delinsCT
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