Canonical Allele Identifier: CA112916439
Gene:
MyVariant.info:
GRCh38 chr5:g.1296306C>T
GRCh37 chr5:g.1296421C>T
gnomAD v2:
5:1296421 C / T
gnomAD v3:
5:1296306 C / T
gnomAD v4:
chr5-1296306-C-T
Joint Max Group AF 0.00089403 (AFR)
Genomes Max Group AF 0.00089403 (AFR)
dbSNP:
36081204
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.1296306C>T , CM000667.2:g.1296306C>T GRCh38
NC_000005.9:g.1296421C>T , CM000667.1:g.1296421C>T GRCh37
NC_000005.8:g.1349421C>T NCBI36
NG_009265.1:g.3742G>A , LRG_343:g.3742G>A
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