ClinGen Allele Registry
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Canonical Allele Identifier:
CA819231234
Gene: TARID
HGNC
NCBI
Linked Data
dbSNP Id:
rs1304754095
gnomAD v3:
6-133875538-T-C
gnomAD v4:
6-133875538-T-C
MyVariant Identifiers:
chr6:g.134196676T>C (hg19)
chr6:g.133875538T>C (hg38)
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000006.12:g.133875538T>C , CM000668.2:g.133875538T>C
GRCh38
NC_000006.11:g.134196676T>C , CM000668.1:g.134196676T>C
GRCh37
NC_000006.10:g.134238369T>C
NCBI36
Transcript Alleles
HGVS
Amino-acid Change
NR_109982.1:n.403+13066A>G
Search 100 bp 5'
Search 100 bp 3'