Canonical Allele Identifier: CA1948012279
Gene: TH HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.2171885_2171886delinsTC , CM000673.2:g.2171885_2171886delinsTC GRCh38
NC_000011.9:g.2193115_2193116delinsTC , CM000673.1:g.2193115_2193116delinsTC GRCh37
NC_000011.8:g.2149691_2149692delinsTC NCBI36
NG_008128.1:g.4920_4921delinsGA

Transcript Alleles

HGVS Amino-acid Change
XM_011520335.1:c.-100_-99delinsGA XP_011518637.1:n.-100_-99delinsGA
XM_011520335.2:c.-100_-99delinsGA XP_011518637.1:n.-100_-99delinsGA
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