Canonical Allele Identifier: CA12494895
Gene:
MyVariant.info:
GRCh38 chr7:g.4371578G>A
GRCh37 chr7:g.4411209G>A
gnomAD v2:
7:4411209 G / A
gnomAD v3:
7:4371578 G / A
gnomAD v4:
chr7-4371578-G-A
Joint Max Group AF 0.41483659 (EAS)
Genomes Max Group AF 0.41483659 (EAS)
dbSNP:
10488360
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.4371578G>A , CM000669.2:g.4371578G>A GRCh38
NC_000007.13:g.4411209G>A , CM000669.1:g.4411209G>A GRCh37
NC_000007.12:g.4377735G>A NCBI36
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