Canonical Allele Identifier: CA1665203009
Gene: TARID HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.133875512A= , CM000668.2:g.133875512A= GRCh38
NC_000006.11:g.134196650A= , CM000668.1:g.134196650A= GRCh37
NC_000006.10:g.134238343A= NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_109982.1:n.403+13092T=