Canonical Allele Identifier: CA680793891

Gene:

Linked Data

• dbSNP Id: rs1201226191
• gnomAD v3: 11-81143497-A-G
• gnomAD v4: 11-81143497-A-G
• MyVariant Identifiers: chr11:g.80854540A>G (hg19) ; chr11:g.81143497A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.81143497A>G , CM000673.2:g.81143497A>G	GRCh38
NC_000011.9:g.80854540A>G , CM000673.1:g.80854540A>G	GRCh37
NC_000011.8:g.80532188A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_247272.2:n.46+109429T>C