Canonical Allele Identifier: CA226767351

Gene:

Linked Data

• dbSNP Id: rs998390145
• MyVariant Identifiers: chr11:g.90779565C>T (hg19) ; chr11:g.91046397C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.91046397C>T , CM000673.2:g.91046397C>T	GRCh38
NC_000011.9:g.90779565C>T , CM000673.1:g.90779565C>T	GRCh37
NC_000011.8:g.90419213C>T	NCBI36