Canonical Allele Identifier: CA597500511

Gene:

Linked Data

• dbSNP Id: rs913931328
• gnomAD v2: 11-20684037-T-G
• gnomAD v3: 11-20662491-T-G
• gnomAD v4: 11-20662491-T-G
• MyVariant Identifiers: chr11:g.20684037T>G (hg19) ; chr11:g.20662491T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.20662491T>G , CM000673.2:g.20662491T>G	GRCh38
NC_000011.9:g.20684037T>G , CM000673.1:g.20684037T>G	GRCh37
NC_000011.8:g.20640613T>G	NCBI36