ClinGen Allele Registry
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Canonical Allele Identifier:
CA846955628
Gene:
Linked Data
dbSNP Id:
rs191977671
MyVariant Identifiers:
chr8:g.126486383C>T (hg19)
chr8:g.125474141C>T (hg38)
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000008.11:g.125474141C>T , CM000670.2:g.125474141C>T
GRCh38
NC_000008.10:g.126486383C>T , CM000670.1:g.126486383C>T
GRCh37
NC_000008.9:g.126555565C>T
NCBI36
Transcript Alleles
HGVS
Amino-acid Change
XR_928628.1:n.256+827C>T
Search 100 bp 5'
Search 100 bp 3'