Canonical Allele Identifier: CA2712993548
Gene: TARID HGNC NCBI

Linked Data

dbSNP Id: rs2114543733

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.133875576T>G , CM000668.2:g.133875576T>G GRCh38
NC_000006.11:g.134196714T>G , CM000668.1:g.134196714T>G GRCh37
NC_000006.10:g.134238407T>G NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_109982.1:n.403+13028A>C