Canonical Allele Identifier: CA1665203003
Gene: TARID HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.133875497G= , CM000668.2:g.133875497G= GRCh38
NC_000006.11:g.134196635G= , CM000668.1:g.134196635G= GRCh37
NC_000006.10:g.134238328G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_109982.1:n.403+13107C=