Canonical Allele Identifier: CA14696732
Gene:
MyVariant.info:
GRCh38 chr19:g.10286727C>T
GRCh37 chr19:g.10397403C>T
gnomAD v2:
19:10397403 C / T
gnomAD v3:
19:10286727 C / T
gnomAD v4:
chr19-10286727-C-T
Joint Max Group AF 0.49454758 (AMR)
Genomes Max Group AF 0.48406941 (AMR)
Exomes Max Group AF 0.50938016 (AMR)
dbSNP:
3093030
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.10286727C>T , CM000681.2:g.10286727C>T GRCh38
NC_000019.9:g.10397403C>T , CM000681.1:g.10397403C>T GRCh37
NC_000019.8:g.10258403C>T NCBI36
NG_007728.1:g.4754C>T
NG_012083.1:g.20887C>T
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