Canonical Allele Identifier: CA2611984821
Gene: TH HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.2171947_2171950del , CM000673.2:g.2171947_2171950del GRCh38
NC_000011.9:g.2193177_2193180del , CM000673.1:g.2193177_2193180del GRCh37
NC_000011.8:g.2149753_2149756del NCBI36
NG_008128.1:g.4860_4863del

Transcript Alleles

HGVS Amino-acid Change
XM_011520335.1:c.-160_-157del XP_011518637.1:n.-160_-157del
XM_011520335.2:c.-160_-157del XP_011518637.1:n.-160_-157del