Canonical Allele Identifier: CA797796567
Gene:
MyVariant.info:
GRCh38 chr4:g.68672197T>A
GRCh37 chr4:g.69537915T>A
gnomAD v3:
4:68672197 T / A
gnomAD v4:
chr4-68672197-T-A
Joint Max Group AF 0.00000802 (AFR)
Genomes Max Group AF 0.00000802 (AFR)
dbSNP:
7686914
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.68672197T>A , CM000666.2:g.68672197T>A GRCh38
NC_000004.11:g.69537915T>A , CM000666.1:g.69537915T>A GRCh37
NC_000004.10:g.69220510T>A NCBI36
NG_052676.1:g.3580A>T
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