Canonical Allele Identifier: CA1665063889
Gene: TARID HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.133539207A= , CM000668.2:g.133539207A= GRCh38
NC_000006.11:g.133860345A= , CM000668.1:g.133860345A= GRCh37
NC_000006.10:g.133902038A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_109982.1:n.707-1849T=