Canonical Allele Identifier: CA303995931
Gene:
MyVariant.info:
GRCh38 chr19:g.1106939T>C
GRCh37 chr19:g.1106938T>C
gnomAD v3:
19:1106939 T / C
gnomAD v4:
chr19-1106939-T-C
Joint Max Group AF 0.00002101 (NFE)
Genomes Max Group AF 0.00000488 (NFE)
Exomes Max Group AF 0.00002108 (NFE)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1106939T>C , CM000681.2:g.1106939T>C GRCh38
NC_000019.9:g.1106938T>C , CM000681.1:g.1106938T>C GRCh37
NC_000019.8:g.1057938T>C NCBI36
NG_050621.1:g.8014T>C
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