Canonical Allele Identifier: CA599168855

Gene:

Linked Data

• dbSNP Id: rs1445543619
• gnomAD v2: 11-45528203-C-T
• gnomAD v3: 11-45506653-C-T
• gnomAD v4: 11-45506653-C-T
• MyVariant Identifiers: chr11:g.45528203C>T (hg19) ; chr11:g.45506653C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.45506653C>T , CM000673.2:g.45506653C>T	GRCh38
NC_000011.9:g.45528203C>T , CM000673.1:g.45528203C>T	GRCh37
NC_000011.8:g.45484779C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_001748204.2:n.909-16882G>A
XR_931245.3:n.566-16882G>A