Canonical Allele Identifier: CA819231201
Gene: TARID HGNC NCBI

Linked Data

dbSNP Id: rs949534880

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.133875477A>G , CM000668.2:g.133875477A>G GRCh38
NC_000006.11:g.134196615A>G , CM000668.1:g.134196615A>G GRCh37
NC_000006.10:g.134238308A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_109982.1:n.403+13127T>C