Canonical Allele Identifier: CA2611984923
Gene: TH HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.2171978del , CM000673.2:g.2171978del GRCh38
NC_000011.9:g.2193208del , CM000673.1:g.2193208del GRCh37
NC_000011.8:g.2149784del NCBI36
NG_008128.1:g.4828del

Transcript Alleles

HGVS Amino-acid Change
XM_011520335.1:c.-192del XP_011518637.1:n.-192del
XM_011520335.2:c.-192del XP_011518637.1:n.-192del