Canonical Allele Identifier: CA13769729
Gene:

Linked Data

dbSNP Id: rs4026608
gnomAD v2: 12-66394664-C-T
gnomAD v3: 12-66000884-C-T
gnomAD v4: 12-66000884-C-T
MyVariant Identifiers: chr12:g.66394664C>T (hg19) chr12:g.66000884C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.66000884C>T , CM000674.2:g.66000884C>T GRCh38
NC_000012.11:g.66394664C>T , CM000674.1:g.66394664C>T GRCh37
NC_000012.10:g.64680931C>T NCBI36
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