Canonical Allele Identifier: CA37675690

Gene:

Linked Data

• dbSNP Id: rs371111660
• gnomAD v2: 1-218705905-T-G
• gnomAD v3: 1-218532563-T-G
• gnomAD v4: 1-218532563-T-G
• MyVariant Identifiers: chr1:g.218705905T>G (hg19) ; chr1:g.218532563T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.218532563T>G , CM000663.2:g.218532563T>G	GRCh38
NC_000001.10:g.218705905T>G , CM000663.1:g.218705905T>G	GRCh37
NC_000001.9:g.216772528T>G	NCBI36