Canonical Allele Identifier: CA540704661
Gene:
MyVariant.info:
GRCh38 chr3:g.108303G>C
GRCh37 chr3:g.149986G>C
gnomAD v2:
3:149986 G / C
gnomAD v3:
3:108303 G / C
gnomAD v4:
chr3-108303-G-C
Joint Max Group AF 0.00002849 (NFE)
Genomes Max Group AF 0.00002849 (NFE)
dbSNP:
12485321
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Genomic Alleles

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