ClinGen Allele Registry
Allele Registry
Register
Login
Forgot Login?
Canonical Allele Identifier:
CA680186677
Gene:
Linked Data
dbSNP Id:
rs10794338
gnomAD v3:
11-746992-T-A
gnomAD v4:
11-746992-T-A
MyVariant Identifiers:
chr11:g.746992T>A (hg19)
chr11:g.746992T>A (hg38)
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000011.10:g.746992T>A , CM000673.2:g.746992T>A
GRCh38
NC_000011.9:g.746992T>A , CM000673.1:g.746992T>A
GRCh37
NC_000011.8:g.736992T>A
NCBI36
NG_008160.1:g.4561T>A
Transcript Alleles
HGVS
Amino-acid change
XR_930963.1:n.259+143T>A
Search 100 bp 5'
Search 100 bp 3'