Canonical Allele Identifier: CA11793090
Gene:
MyVariant.info:
GRCh38 chr4:g.154562762C>T
GRCh37 chr4:g.155483914C>T
gnomAD v2:
4:155483914 C / T
gnomAD v3:
4:154562762 C / T
gnomAD v4:
chr4-154562762-C-T
Joint Max Group AF 0.53119085 (EAS)
Genomes Max Group AF 0.53119085 (EAS)
ClinVar RCV:
RCV001715022
ClinVar Variation:
1290152
dbSNP:
1800788
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.154562762C>T , CM000666.2:g.154562762C>T GRCh38
NC_000004.11:g.155483914C>T , CM000666.1:g.155483914C>T GRCh37
NC_000004.10:g.155703364C>T NCBI36
NG_008833.1:g.4783C>T , LRG_558:g.4783C>T
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