ClinGen Allele Registry
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Canonical Allele Identifier:
CA148431575
Gene: TARID
HGNC
NCBI
Linked Data
dbSNP Id:
rs892693804
MyVariant Identifiers:
chr6:g.134196721A>G (hg19)
chr6:g.133875583A>G (hg38)
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000006.12:g.133875583A>G , CM000668.2:g.133875583A>G
GRCh38
NC_000006.11:g.134196721A>G , CM000668.1:g.134196721A>G
GRCh37
NC_000006.10:g.134238414A>G
NCBI36
Transcript Alleles
HGVS
Amino-acid Change
NR_109982.1:n.403+13021T>C
Search 100 bp 5'
Search 100 bp 3'