Canonical Allele Identifier: CA2841197871
Gene: TH HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.2171857G>C , CM000673.2:g.2171857G>C GRCh38
NC_000011.9:g.2193087G>C , CM000673.1:g.2193087G>C GRCh37
NC_000011.8:g.2149663G>C NCBI36
NG_008128.1:g.4949C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000352909.7:c.-71C>G ENSP00000325951.3:n.-71C>G
XM_011520335.1:c.-71C>G XP_011518637.1:n.-71C>G
XM_011520335.2:c.-71C>G XP_011518637.1:n.-71C>G
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