Canonical Allele Identifier: CA12231313
Gene:
MyVariant.info:
GRCh38 chr6:g.31575324G>A
GRCh37 chr6:g.31543101G>A
gnomAD v2:
6:31543101 G / A
gnomAD v3:
6:31575324 G / A
gnomAD v4:
chr6-31575324-G-A
Joint Max Group AF 0.05784956 (SAS)
Genomes Max Group AF 0.05884625 (SAS)
Exomes Max Group AF 0.0573612 (SAS)
ClinVar RCV:
RCV001354057
RCV001836995
ClinVar Variation:
1048804
dbSNP:
361525
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31575324G>A , CM000668.2:g.31575324G>A GRCh38
NC_000006.11:g.31543101G>A , CM000668.1:g.31543101G>A GRCh37
NC_000006.10:g.31651080G>A NCBI36
NG_007462.1:g.4752G>A
NG_012010.1:g.8226G>A
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