Canonical Allele Identifier: CA1948012493
Gene: TH HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.2172052_2172055delinsCTCG , CM000673.2:g.2172052_2172055delinsCTCG GRCh38
NC_000011.9:g.2193282_2193285delinsCTCG , CM000673.1:g.2193282_2193285delinsCTCG GRCh37
NC_000011.8:g.2149858_2149861delinsCTCG NCBI36
NG_008128.1:g.4751_4754delinsCGAG

Transcript Alleles

HGVS Amino-acid Change
XM_011520335.1:c.-269_-266delinsCGAG XP_011518637.1:n.-269_-266delinsCGAG
XM_011520335.2:c.-269_-266delinsCGAG XP_011518637.1:n.-269_-266delinsCGAG
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