Canonical Allele Identifier: CA11393971
Gene:
MyVariant.info:
GRCh38 chr3:g.108303G>A
GRCh37 chr3:g.149986G>A
gnomAD v2:
3:149986 G / A
gnomAD v3:
3:108303 G / A
gnomAD v4:
chr3-108303-G-A
Joint Max Group AF 0.46907626 (MID)
Genomes Max Group AF 0.4194468 (NFE)
dbSNP:
12485321
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.108303G>A , CM000665.2:g.108303G>A GRCh38
NC_000003.11:g.149986G>A , CM000665.1:g.149986G>A GRCh37
NC_000003.10:g.124986G>A NCBI36
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