ClinGen Allele Registry
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Canonical Allele Identifier:
CA50232849
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr2:g.67746755T>G
GRCh37
chr2:g.67973887T>G
Linked Data - Sequence & Population
gnomAD v2:
2:67973887 T / G
gnomAD v3:
2:67746755 T / G
gnomAD v4:
chr2-67746755-T-G
Joint Max Group AF
0.10483246 (AFR)
Genomes Max Group AF
0.10483246 (AFR)
Linked Data - NCBI & NCI
dbSNP:
13432159
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000002.12:g.67746755T>G , CM000664.2:g.67746755T>G
GRCh38
NC_000002.11:g.67973887T>G , CM000664.1:g.67973887T>G
GRCh37
NC_000002.10:g.67827391T>G
NCBI36
Search 100 bp 5'
Search 100 bp 3'