ClinGen Allele Registry
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Canonical Allele Identifier:
CA12231312
Gene:
Linked Data
ClinVar Variation Id:
12389
ClinVar RCV Id:
RCV000013196
RCV000013197
dbSNP Id:
rs1799724
gnomAD v2:
6-31542482-C-T
gnomAD v3:
6-31574705-C-T
gnomAD v4:
6-31574705-C-T
MyVariant Identifiers:
chr6:g.31542482C>T (hg19)
chr6:g.31574705C>T (hg38)
PubMed:
PMID:11273064
PMID:15895461
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000006.12:g.31574705C>T , CM000668.2:g.31574705C>T
GRCh38
NC_000006.11:g.31542482C>T , CM000668.1:g.31542482C>T
GRCh37
NC_000006.10:g.31650461C>T
NCBI36
NG_007462.1:g.4133C>T
NG_012010.1:g.7607C>T
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