Canonical Allele Identifier: CA12321089
Gene:
MyVariant.info:
GRCh38 chr6:g.31826815C>T
GRCh37 chr6:g.31794592C>T
gnomAD v2:
6:31794592 C / T
gnomAD v3:
6:31826815 C / T
gnomAD v4:
chr6-31826815-C-T
Joint Max Group AF 0.64611778 (AFR)
Genomes Max Group AF 0.64611778 (AFR)
ClinVar Allele:
682506
ClinVar RCV:
RCV000856579
ClinVar Variation:
694519
dbSNP:
2763979
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31826815C>T , CM000668.2:g.31826815C>T GRCh38
NC_000006.11:g.31794592C>T , CM000668.1:g.31794592C>T GRCh37
NC_000006.10:g.31902571C>T NCBI36
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