Canonical Allele Identifier: CA11957814
Gene:
MyVariant.info:
GRCh38 chr5:g.1299910G>T
GRCh37 chr5:g.1300025G>T
gnomAD v2:
5:1300025 G / T
gnomAD v3:
5:1299910 G / T
gnomAD v4:
chr5-1299910-G-T
Joint Max Group AF 0.49629105 (AFR)
Genomes Max Group AF 0.49629105 (AFR)
dbSNP:
2853668
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.1299910G>T , CM000667.2:g.1299910G>T GRCh38
NC_000005.9:g.1300025G>T , CM000667.1:g.1300025G>T GRCh37
NC_000005.8:g.1353025G>T NCBI36
NG_009265.1:g.138C>A , LRG_343:g.138C>A
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