ClinGen Allele Registry
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Canonical Allele Identifier:
CA846955622
Gene:
Linked Data
dbSNP Id:
rs1297134938
gnomAD v3:
8-125474096-T-C
gnomAD v4:
8-125474096-T-C
MyVariant Identifiers:
chr8:g.126486338T>C (hg19)
chr8:g.125474096T>C (hg38)
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000008.11:g.125474096T>C , CM000670.2:g.125474096T>C
GRCh38
NC_000008.10:g.126486338T>C , CM000670.1:g.126486338T>C
GRCh37
NC_000008.9:g.126555520T>C
NCBI36
Transcript Alleles
HGVS
Amino-acid Change
XR_928628.1:n.256+782T>C
Search 100 bp 5'
Search 100 bp 3'