Canonical Allele Identifier: CA11123792
Gene:

Linked Data

dbSNP Id: rs2048874
gnomAD v2: 2-113523967-C-T
gnomAD v3: 2-112766390-C-T
gnomAD v4: 2-112766390-C-T
MyVariant Identifiers: chr2:g.113523967C>T (hg19) chr2:g.112766390C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.112766390C>T , CM000664.2:g.112766390C>T GRCh38
NC_000002.11:g.113523967C>T , CM000664.1:g.113523967C>T GRCh37
NC_000002.10:g.113240438C>T NCBI36
NG_041820.1:g.3288G>A
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