ClinGen Allele Registry
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Canonical Allele Identifier:
CA846959178
Gene:
Linked Data
dbSNP Id:
rs1364281166
gnomAD v2:
8-126490883-C-T
gnomAD v3:
8-125478641-C-T
gnomAD v4:
8-125478641-C-T
MyVariant Identifiers:
chr8:g.126490883C>T (hg19)
chr8:g.125478641C>T (hg38)
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000008.11:g.125478641C>T , CM000670.2:g.125478641C>T
GRCh38
NC_000008.10:g.126490883C>T , CM000670.1:g.126490883C>T
GRCh37
NC_000008.9:g.126560065C>T
NCBI36
Transcript Alleles
HGVS
Amino-acid Change
XR_928628.1:n.256+5327C>T
Search 100 bp 5'
Search 100 bp 3'