Canonical Allele Identifier: CA10654670
Gene:
MyVariant.info:
GRCh38 chr4:g.154604124G>A
GRCh37 chr4:g.155525276G>A
gnomAD v2:
4:155525276 G / A
gnomAD v3:
4:154604124 G / A
gnomAD v4:
chr4-154604124-G-A
Joint Max Group AF 0.47152026 (EAS)
Genomes Max Group AF 0.43096026 (EAS)
Exomes Max Group AF 0.47850755 (EAS)
ClinVar RCV:
RCV000361528
RCV001643130
ClinVar Variation:
369438
dbSNP:
2066865
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.154604124G>A , CM000666.2:g.154604124G>A GRCh38
NC_000004.11:g.155525276G>A , CM000666.1:g.155525276G>A GRCh37
NC_000004.10:g.155744726G>A NCBI36
NG_008834.1:g.13627C>T
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