Canonical Allele Identifier: CA11993107
Gene:
MyVariant.info:
GRCh38 chr5:g.1249479T>A
GRCh37 chr5:g.1249594T>A
gnomAD v2:
5:1249594 T / A
gnomAD v3:
5:1249479 T / A
gnomAD v4:
chr5-1249479-T-A
Joint Max Group AF 0.38037832 (MID)
Genomes Max Group AF 0.33870205 (NFE)
dbSNP:
10078761
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.1249479T>A , CM000667.2:g.1249479T>A GRCh38
NC_000005.9:g.1249594T>A , CM000667.1:g.1249594T>A GRCh37
NC_000005.8:g.1302594T>A NCBI36
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