Canonical Allele Identifier: CA603661008

Gene:

Linked Data

• dbSNP Id: rs1298559459
• gnomAD v2: 12-21402963-G-A
• gnomAD v3: 12-21250029-G-A
• gnomAD v4: 12-21250029-G-A
• MyVariant Identifiers: chr12:g.21402963G>A (hg19) ; chr12:g.21250029G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.21250029G>A , CM000674.2:g.21250029G>A	GRCh38
NC_000012.11:g.21402963G>A , CM000674.1:g.21402963G>A	GRCh37
NC_000012.10:g.21294230G>A	NCBI36