Canonical Allele Identifier: CA11295663

Gene:

Linked Data

• dbSNP Id: rs1516092
• gnomAD v2: 2-161757141-A-G
• gnomAD v3: 2-160900630-A-G
• gnomAD v4: 2-160900630-A-G
• MyVariant Identifiers: chr2:g.161757141A>G (hg19) ; chr2:g.160900630A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.160900630A>G , CM000664.2:g.160900630A>G	GRCh38
NC_000002.11:g.161757141A>G , CM000664.1:g.161757141A>G	GRCh37
NC_000002.10:g.161465387A>G	NCBI36