ClinGen Allele Registry
Allele Registry
Register
Login
Forgot Login?
Canonical Allele Identifier:
CA669472802
Gene:
Linked Data
dbSNP Id:
rs1409048536
MyVariant Identifiers:
chr10:g.8739400T>A (hg19)
chr10:g.8697437T>A (hg38)
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000010.11:g.8697437T>A , CM000672.2:g.8697437T>A
GRCh38
NC_000010.10:g.8739400T>A , CM000672.1:g.8739400T>A
GRCh37
NC_000010.9:g.8779406T>A
NCBI36
Transcript Alleles
HGVS
Amino-acid Change
XR_930641.1:n.33-27636A>T
Search 100 bp 5'
Search 100 bp 3'