ClinGen Allele Registry
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Canonical Allele Identifier:
CA13214168
Gene:
Linked Data
dbSNP Id:
rs11255841
gnomAD v2:
10-8739580-T-A
gnomAD v3:
10-8697617-T-A
gnomAD v4:
10-8697617-T-A
MyVariant Identifiers:
chr10:g.8739580T>A (hg19)
chr10:g.8697617T>A (hg38)
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000010.11:g.8697617T>A , CM000672.2:g.8697617T>A
GRCh38
NC_000010.10:g.8739580T>A , CM000672.1:g.8739580T>A
GRCh37
NC_000010.9:g.8779586T>A
NCBI36
Transcript Alleles
HGVS
Amino-acid change
XR_930641.1:n.33-27816A>T
Search 100 bp 5'
Search 100 bp 3'