Canonical Allele Identifier: CA13719118
Gene:
MyVariant.info:
GRCh38 chr12:g.666033G>A
GRCh37 chr12:g.775199G>A
gnomAD v2:
12:775199 G / A
gnomAD v3:
12:666033 G / A
gnomAD v4:
chr12-666033-G-A
Joint Max Group AF 0.34571708 (SAS)
Genomes Max Group AF 0.34571708 (SAS)
dbSNP:
11833579
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.666033G>A , CM000674.2:g.666033G>A GRCh38
NC_000012.11:g.775199G>A , CM000674.1:g.775199G>A GRCh37
NC_000012.10:g.645460G>A NCBI36
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