Canonical Allele Identifier: CA676911679

Gene:

Linked Data

• dbSNP Id: rs1307343919
• MyVariant Identifiers: chr11:g.45528143C>A (hg19) ; chr11:g.45506593C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.45506593C>A , CM000673.2:g.45506593C>A	GRCh38
NC_000011.9:g.45528143C>A , CM000673.1:g.45528143C>A	GRCh37
NC_000011.8:g.45484719C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_001748204.2:n.909-16822G>T
XR_931245.3:n.566-16822G>T