Canonical Allele Identifier: CA2611985028
Gene: TH HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.2172008del , CM000673.2:g.2172008del GRCh38
NC_000011.9:g.2193238del , CM000673.1:g.2193238del GRCh37
NC_000011.8:g.2149814del NCBI36
NG_008128.1:g.4800del

Transcript Alleles

HGVS Amino-acid Change
XM_011520335.1:c.-220del XP_011518637.1:n.-220del
XM_011520335.2:c.-220del XP_011518637.1:n.-220del