Canonical Allele Identifier: CA178436373
Gene:
MyVariant.info:
GRCh38 chr8:g.66178947G>T
GRCh37 chr8:g.67091182G>T
gnomAD v2:
8:67091182 G / T
gnomAD v3:
8:66178947 G / T
gnomAD v4:
chr8-66178947-G-T
Joint Max Group AF 0.06090042 (NFE)
Genomes Max Group AF 0.06090042 (NFE)
ClinVar RCV:
RCV000033935
RCV003894839
ClinVar Variation:
38800
dbSNP:
12721510
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.66178947G>T , CM000670.2:g.66178947G>T GRCh38
NC_000008.10:g.67091182G>T , CM000670.1:g.67091182G>T GRCh37
NC_000008.9:g.67253736G>T NCBI36
NG_016127.1:g.4517C>A
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