Canonical Allele Identifier: CA12231312
Gene:
MyVariant.info:
GRCh38 chr6:g.31574705C>T
GRCh37 chr6:g.31542482C>T
gnomAD v2:
6:31542482 C / T
gnomAD v3:
6:31574705 C / T
gnomAD v4:
chr6-31574705-C-T
Joint Max Group AF 0.16691903 (AMR)
Genomes Max Group AF 0.16691903 (AMR)
ClinVar RCV:
RCV000013196
RCV000013197
ClinVar Variation:
12389
dbSNP:
1799724
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31574705C>T , CM000668.2:g.31574705C>T GRCh38
NC_000006.11:g.31542482C>T , CM000668.1:g.31542482C>T GRCh37
NC_000006.10:g.31650461C>T NCBI36
NG_007462.1:g.4133C>T
NG_012010.1:g.7607C>T
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