Canonical Allele Identifier: CA12221124
Gene:
MyVariant.info:
GRCh38 chr6:g.426155G>C
GRCh37 chr6:g.426155G>C
gnomAD v2:
6:426155 G / C
gnomAD v3:
6:426155 G / C
gnomAD v4:
chr6-426155-G-C
Joint Max Group AF 0.62873801 (NFE)
Genomes Max Group AF 0.62873801 (NFE)
dbSNP:
9378815
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.426155G>C , CM000668.2:g.426155G>C GRCh38
NC_000006.11:g.426155G>C , CM000668.1:g.426155G>C GRCh37
NC_000006.10:g.371155G>C NCBI36
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