Canonical Allele Identifier: CA136866012
Gene:
MyVariant.info:
GRCh38 chr6:g.31575186G>A
GRCh37 chr6:g.31542963G>A
gnomAD v2:
6:31542963 G / A
gnomAD v3:
6:31575186 G / A
gnomAD v4:
chr6-31575186-G-A
Joint Max Group AF 0.02267421 (AMR)
Genomes Max Group AF 0.02354209 (AMR)
Exomes Max Group AF 0.02139357 (AMR)
ClinVar RCV:
RCV000013188
ClinVar Variation:
12387
dbSNP:
1800750
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31575186G>A , CM000668.2:g.31575186G>A GRCh38
NC_000006.11:g.31542963G>A , CM000668.1:g.31542963G>A GRCh37
NC_000006.10:g.31650942G>A NCBI36
NG_007462.1:g.4614G>A
NG_012010.1:g.8088G>A
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