Canonical Allele Identifier: CA770673166
Gene:
MyVariant.info:
GRCh38 chr2:g.59075742T>G
GRCh37 chr2:g.59302877T>G
gnomAD v3:
2:59075742 T / G
gnomAD v4:
chr2-59075742-T-G
Joint Max Group AF 0.00003246 (AFR)
Genomes Max Group AF 0.00003246 (AFR)
dbSNP:
887912
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.59075742T>G , CM000664.2:g.59075742T>G GRCh38
NC_000002.11:g.59302877T>G , CM000664.1:g.59302877T>G GRCh37
NC_000002.10:g.59156381T>G NCBI36
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