Canonical Allele Identifier: CA2580593520
Gene: TARID HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.133875536C>G , CM000668.2:g.133875536C>G GRCh38
NC_000006.11:g.134196674C>G , CM000668.1:g.134196674C>G GRCh37
NC_000006.10:g.134238367C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_109982.1:n.403+13068G>C