Canonical Allele Identifier: CA12266081
Gene:
MyVariant.info:
GRCh38 chr6:g.31574699C>A
GRCh37 chr6:g.31542476C>A
gnomAD v2:
6:31542476 C / A
gnomAD v3:
6:31574699 C / A
gnomAD v4:
chr6-31574699-C-A
Joint Max Group AF 0.24445204 (SAS)
Genomes Max Group AF 0.24445204 (SAS)
ClinVar RCV:
RCV000013198
ClinVar Variation:
12390
dbSNP:
1800630
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31574699C>A , CM000668.2:g.31574699C>A GRCh38
NC_000006.11:g.31542476C>A , CM000668.1:g.31542476C>A GRCh37
NC_000006.10:g.31650455C>A NCBI36
NG_007462.1:g.4127C>A
NG_012010.1:g.7601C>A
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