Canonical Allele Identifier: CA11492093
Gene:
MyVariant.info:
GRCh38 chr3:g.1700081G>C
GRCh37 chr3:g.1741765G>C
gnomAD v2:
3:1741765 G / C
gnomAD v3:
3:1700081 G / C
gnomAD v4:
chr3-1700081-G-C
Joint Max Group AF 0.14317246 (NFE)
Genomes Max Group AF 0.14317246 (NFE)
dbSNP:
73001827
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.1700081G>C , CM000665.2:g.1700081G>C GRCh38
NC_000003.11:g.1741765G>C , CM000665.1:g.1741765G>C GRCh37
NC_000003.10:g.1716765G>C NCBI36
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