Canonical Allele Identifier: CA1665203029
Gene: TARID HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.133875538T= , CM000668.2:g.133875538T= GRCh38
NC_000006.11:g.134196676T= , CM000668.1:g.134196676T= GRCh37
NC_000006.10:g.134238369T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_109982.1:n.403+13066A=