Canonical Allele Identifier: CA11685762
Gene:
dbSNP:
10008492
gnomAD v2:
4:38765720 C / T
gnomAD v3:
4:38764099 C / T
gnomAD v4:
chr4-38764099-C-T
Joint Max Group AF 0.97440998 (EAS)
Genomes Max Group AF 0.97440998 (EAS)
MyVariant.info:
GRCh38 chr4:g.38764099C>T
GRCh37 chr4:g.38765720C>T
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.38764099C>T , CM000666.2:g.38764099C>T GRCh38
NC_000004.11:g.38765720C>T , CM000666.1:g.38765720C>T GRCh37
NC_000004.10:g.38442115C>T NCBI36
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