Canonical Allele Identifier: CA2712993546
Gene: TARID HGNC NCBI

Linked Data

dbSNP Id: rs2114543710

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.133875543C>T , CM000668.2:g.133875543C>T GRCh38
NC_000006.11:g.134196681C>T , CM000668.1:g.134196681C>T GRCh37
NC_000006.10:g.134238374C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_109982.1:n.403+13061G>A