Canonical Allele Identifier: CA15077767
Gene:
MyVariant.info:
GRCh38 chr1:g.55038977G>A
GRCh37 chr1:g.55504650G>A
gnomAD v2:
1:55504650 G / A
gnomAD v3:
1:55038977 G / A
gnomAD v4:
chr1-55038977-G-A
Joint Max Group AF 0.73318722 (AFR)
Genomes Max Group AF 0.73318722 (AFR)
ClinVar RCV:
RCV000508949
ClinVar Variation:
440703
dbSNP:
2479409
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.55038977G>A , CM000663.2:g.55038977G>A GRCh38
NC_000001.10:g.55504650G>A , CM000663.1:g.55504650G>A GRCh37
NC_000001.9:g.55277238G>A NCBI36
NG_009061.1:g.4431G>A , LRG_275:g.4431G>A
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