Canonical Allele Identifier: CA12002015
Gene:
MyVariant.info:
GRCh38 chr5:g.63962738C>G
GRCh37 chr5:g.63258565C>G
gnomAD v2:
5:63258565 C / G
gnomAD v3:
5:63962738 C / G
gnomAD v4:
chr5-63962738-C-G
Joint Max Group AF 0.73725461 (EAS)
Genomes Max Group AF 0.73725461 (EAS)
ClinVar RCV:
RCV000603722
ClinVar Variation:
375667
dbSNP:
6295
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.63962738C>G , CM000667.2:g.63962738C>G GRCh38
NC_000005.9:g.63258565C>G , CM000667.1:g.63258565C>G GRCh37
NC_000005.8:g.63294321C>G NCBI36
NG_032816.1:g.4555G>C
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