ClinGen Allele Registry
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Canonical Allele Identifier:
CA220846362
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr11:g.37849431T>C
GRCh37
chr11:g.37870981T>C
Linked Data - Sequence & Population
gnomAD v2:
11:37870981 T / C
gnomAD v3:
11:37849431 T / C
gnomAD v4:
chr11-37849431-T-C
Joint Max Group AF
0.32383115 (AFR)
Genomes Max Group AF
0.32383115 (AFR)
Linked Data - NCBI & NCI
dbSNP:
16930685
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000011.10:g.37849431T>C , CM000673.2:g.37849431T>C
GRCh38
NC_000011.9:g.37870981T>C , CM000673.1:g.37870981T>C
GRCh37
NC_000011.8:g.37827557T>C
NCBI36
Search 100 bp 5'
Search 100 bp 3'