Canonical Allele Identifier: CA2611984641
Gene: TH HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.2171903del , CM000673.2:g.2171903del GRCh38
NC_000011.9:g.2193133del , CM000673.1:g.2193133del GRCh37
NC_000011.8:g.2149709del NCBI36
NG_008128.1:g.4907del

Transcript Alleles

HGVS Amino-acid Change
XM_011520335.1:c.-113del XP_011518637.1:n.-113del
XM_011520335.2:c.-113del XP_011518637.1:n.-113del