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)

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