ClinGen Allele Registry
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Canonical Allele Identifier:
CA857362222
Gene:
Linked Data
dbSNP Id:
rs1218396287
gnomAD v3:
8-97269725-T-C
gnomAD v4:
8-97269725-T-C
MyVariant Identifiers:
chr8:g.98281953T>C (hg19)
chr8:g.97269725T>C (hg38)
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000008.11:g.97269725T>C , CM000670.2:g.97269725T>C
GRCh38
NC_000008.10:g.98281953T>C , CM000670.1:g.98281953T>C
GRCh37
NC_000008.9:g.98351129T>C
NCBI36
Transcript Alleles
HGVS
Amino-acid Change
NR_125390.1:n.471+149345A>G
Search 100 bp 5'
Search 100 bp 3'