Canonical Allele Identifier: CA112973389
Gene:
MyVariant.info:
GRCh38 chr5:g.1447647G>C
GRCh37 chr5:g.1447762G>C
gnomAD v2:
5:1447762 G / C
gnomAD v3:
5:1447647 G / C
gnomAD v4:
chr5-1447647-G-C
Joint Max Group AF 0.09377672 (NFE)
Genomes Max Group AF 0.09377672 (NFE)
dbSNP:
11564750
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.1447647G>C , CM000667.2:g.1447647G>C GRCh38
NC_000005.9:g.1447762G>C , CM000667.1:g.1447762G>C GRCh37
NC_000005.8:g.1500762G>C NCBI36
NG_015885.1:g.2782C>G
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