Canonical Allele Identifier: CA2611984561
Gene: TH HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.2171880dup , CM000673.2:g.2171880dup GRCh38
NC_000011.9:g.2193110dup , CM000673.1:g.2193110dup GRCh37
NC_000011.8:g.2149686dup NCBI36
NG_008128.1:g.4930dup

Transcript Alleles

HGVS Amino-acid Change
XM_011520335.1:c.-90dup XP_011518637.1:n.-90dup
XM_011520335.2:c.-90dup XP_011518637.1:n.-90dup