Canonical Allele Identifier: CA13680396
Gene:
MyVariant.info:
GRCh38 chr12:g.664290C>T
GRCh37 chr12:g.773456C>T
gnomAD v2:
12:773456 C / T
gnomAD v3:
12:664290 C / T
gnomAD v4:
chr12-664290-C-T
Joint Max Group AF 0.37670364 (NFE)
Genomes Max Group AF 0.37670364 (NFE)
dbSNP:
3809263
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.664290C>T , CM000674.2:g.664290C>T GRCh38
NC_000012.11:g.773456C>T , CM000674.1:g.773456C>T GRCh37
NC_000012.10:g.643717C>T NCBI36
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