Canonical Allele Identifier: CA2611985083
Gene: TH HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.2172028_2172039del , CM000673.2:g.2172028_2172039del GRCh38
NC_000011.9:g.2193258_2193269del , CM000673.1:g.2193258_2193269del GRCh37
NC_000011.8:g.2149834_2149845del NCBI36
NG_008128.1:g.4769_4780del

Transcript Alleles

HGVS Amino-acid Change
XM_011520335.1:c.-251_-240del XP_011518637.1:n.-251_-240del
XM_011520335.2:c.-251_-240del XP_011518637.1:n.-251_-240del