ClinGen Allele Registry
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Canonical Allele Identifier:
CA1665203029
Gene: TARID
HGNC
NCBI
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000006.12:g.133875538T= , CM000668.2:g.133875538T=
GRCh38
NC_000006.11:g.134196676T= , CM000668.1:g.134196676T=
GRCh37
NC_000006.10:g.134238369T=
NCBI36
Transcript Alleles
HGVS
Amino-acid Change
NR_109982.1:n.403+13066A=
Search 100 bp 5'
Search 100 bp 3'