Canonical Allele Identifier: CA1665202982
Gene: TARID HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.133875460C= , CM000668.2:g.133875460C= GRCh38
NC_000006.11:g.134196598C= , CM000668.1:g.134196598C= GRCh37
NC_000006.10:g.134238291C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_109982.1:n.403+13144G=