Canonical Allele Identifier: CA2611984585
Gene: TH HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.2171885del , CM000673.2:g.2171885del GRCh38
NC_000011.9:g.2193115del , CM000673.1:g.2193115del GRCh37
NC_000011.8:g.2149691del NCBI36
NG_008128.1:g.4922del

Transcript Alleles

HGVS Amino-acid Change
XM_011520335.1:c.-98del XP_011518637.1:n.-98del
XM_011520335.2:c.-98del XP_011518637.1:n.-98del