ClinGen Allele Registry
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Canonical Allele Identifier:
CA12321089
Gene:
Linked Data
ClinVar Variation Id:
694519
ClinVar RCV Id:
RCV000856579
dbSNP Id:
rs2763979
gnomAD v2:
6-31794592-C-T
gnomAD v3:
6-31826815-C-T
gnomAD v4:
6-31826815-C-T
MyVariant Identifiers:
chr6:g.31794592C>T (hg19)
chr6:g.31826815C>T (hg38)
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000006.12:g.31826815C>T , CM000668.2:g.31826815C>T
GRCh38
NC_000006.11:g.31794592C>T , CM000668.1:g.31794592C>T
GRCh37
NC_000006.10:g.31902571C>T
NCBI36
Search 100 bp 5'
Search 100 bp 3'