Canonical Allele Identifier: CA222002626

Gene:

Linked Data

• dbSNP Id: rs531804228
• MyVariant Identifiers: chr11:g.45528138A>G (hg19) ; chr11:g.45506588A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.45506588A>G , CM000673.2:g.45506588A>G	GRCh38
NC_000011.9:g.45528138A>G , CM000673.1:g.45528138A>G	GRCh37
NC_000011.8:g.45484714A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_001748204.2:n.909-16817T>C
XR_931245.3:n.566-16817T>C