Canonical Allele Identifier: CA13638383

Gene:

Linked Data

• dbSNP Id: rs5020775
• gnomAD v2: 12-130604847-G-A
• gnomAD v3: 12-130120302-G-A
• gnomAD v4: 12-130120302-G-A
• MyVariant Identifiers: chr12:g.130604847G>A (hg19) ; chr12:g.130120302G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.130120302G>A , CM000674.2:g.130120302G>A	GRCh38
NC_000012.11:g.130604847G>A , CM000674.1:g.130604847G>A	GRCh37
NC_000012.10:g.129170800G>A	NCBI36