Canonical Allele Identifier: CA11245537
Gene:
MyVariant.info:
GRCh38 chr2:g.4271386T>C
GRCh37 chr2:g.4318976T>C
gnomAD v2:
2:4318976 T / C
gnomAD v3:
2:4271386 T / C
gnomAD v4:
chr2-4271386-T-C
Joint Max Group AF 0.13813047 (NFE)
Genomes Max Group AF 0.13813047 (NFE)
dbSNP:
11686135
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.4271386T>C , CM000664.2:g.4271386T>C GRCh38
NC_000002.11:g.4318976T>C , CM000664.1:g.4318976T>C GRCh37
NC_000002.10:g.4296851T>C NCBI36
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