ClinGen Allele Registry
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Canonical Allele Identifier:
CA57901620
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr2:g.145347686T>C
GRCh37
chr2:g.146105254T>C
Linked Data - Sequence & Population
gnomAD v2:
2:146105254 T / C
gnomAD v3:
2:145347686 T / C
gnomAD v4:
chr2-145347686-T-C
Joint Max Group AF
0.36340609 (AFR)
Genomes Max Group AF
0.36340609 (AFR)
Linked Data - NCBI & NCI
dbSNP:
10445672
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000002.12:g.145347686T>C , CM000664.2:g.145347686T>C
GRCh38
NC_000002.11:g.146105254T>C , CM000664.1:g.146105254T>C
GRCh37
NC_000002.10:g.145821724T>C
NCBI36
Search 100 bp 5'
Search 100 bp 3'