Canonical Allele Identifier: CA1948012542
Gene: TH HGNC NCBI

Linked Data

dbSNP Id: rs1846276736

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.2172084del , CM000673.2:g.2172084del GRCh38
NC_000011.9:g.2193314del , CM000673.1:g.2193314del GRCh37
NC_000011.8:g.2149890del NCBI36
NG_008128.1:g.4724del

Transcript Alleles

HGVS Amino-acid Change
XM_011520335.1:c.-296del XP_011518637.1:n.-296del
XM_011520335.2:c.-296del XP_011518637.1:n.-296del