Canonical Allele Identifier: CA1665027927
Gene: TARID HGNC NCBI

Linked Data

dbSNP Id: rs9375969

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.133546664G>C , CM000668.2:g.133546664G>C GRCh38
NC_000006.11:g.133867802G>C , CM000668.1:g.133867802G>C GRCh37
NC_000006.10:g.133909495G>C NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_109982.1:n.707-9306C>G