Canonical Allele Identifier: CA65797314
Gene:

Linked Data

dbSNP Id: rs1014570938
gnomAD v2: 2-217481324-T-C
gnomAD v3: 2-216616601-T-C
gnomAD v4: 2-216616601-T-C
MyVariant Identifiers: chr2:g.217481324T>C (hg19) chr2:g.217481324_217481326delinsCGG (hg19) chr2:g.216616601T>C (hg38) chr2:g.216616601_216616603delinsCGG (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.216616601T>C , CM000664.2:g.216616601T>C GRCh38
NC_000002.11:g.217481324T>C , CM000664.1:g.217481324T>C GRCh37
NC_000002.10:g.217189569T>C NCBI36
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