Canonical Allele Identifier: CA1665203031
Gene: TARID HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.133875546A= , CM000668.2:g.133875546A= GRCh38
NC_000006.11:g.134196684A= , CM000668.1:g.134196684A= GRCh37
NC_000006.10:g.134238377A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_109982.1:n.403+13058T=