Canonical Allele Identifier: CA14722798
Gene:
MyVariant.info:
GRCh38 chr19:g.48758381C>T
GRCh37 chr19:g.49261638C>T
gnomAD v2:
19:49261638 C / T
gnomAD v3:
19:48758381 C / T
gnomAD v4:
chr19-48758381-C-T
Joint Max Group AF 0.54440665 (EAS)
Genomes Max Group AF 0.62538224 (EAS)
Exomes Max Group AF 0.52574275 (EAS)
dbSNP:
3745706
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.48758381C>T , CM000681.2:g.48758381C>T GRCh38
NC_000019.9:g.49261638C>T , CM000681.1:g.49261638C>T GRCh37
NC_000019.8:g.53953450C>T NCBI36
NG_007510.1:g.2010G>A
NG_033945.1:g.7295C>T
NG_007510.2:g.2010G>A
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