Canonical Allele Identifier: CA185710860
Gene:
MyVariant.info:
GRCh38 chr8:g.127179427T>A
GRCh37 chr8:g.128191672T>A
gnomAD v2:
8:128191672 T / A
gnomAD v3:
8:127179427 T / A
gnomAD v4:
chr8-127179427-T-A
Joint Max Group AF 0.00532141 (NFE)
Genomes Max Group AF 0.00532141 (NFE)
ClinVar RCV:
RCV001257963
ClinVar Variation:
979040
dbSNP:
188140481
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.127179427T>A , CM000670.2:g.127179427T>A GRCh38
NC_000008.10:g.128191672T>A , CM000670.1:g.128191672T>A GRCh37
NC_000008.9:g.128260854T>A NCBI36
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