ClinGen Allele Registry
Allele Registry
Register
Login
Forgot Login?
Canonical Allele Identifier:
CA819231257
Gene: TARID
HGNC
NCBI
Linked Data
dbSNP Id:
rs1201778153
gnomAD v3:
6-133875594-A-G
gnomAD v4:
6-133875594-A-G
MyVariant Identifiers:
chr6:g.134196732A>G (hg19)
chr6:g.133875594A>G (hg38)
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000006.12:g.133875594A>G , CM000668.2:g.133875594A>G
GRCh38
NC_000006.11:g.134196732A>G , CM000668.1:g.134196732A>G
GRCh37
NC_000006.10:g.134238425A>G
NCBI36
Transcript Alleles
HGVS
Amino-acid Change
NR_109982.1:n.403+13010T>C
Search 100 bp 5'
Search 100 bp 3'