Canonical Allele Identifier: CA222002624

Gene:

Linked Data

• dbSNP Id: rs112083088
• gnomAD v2: 11-45528111-C-T
• gnomAD v3: 11-45506561-C-T
• gnomAD v4: 11-45506561-C-T
• MyVariant Identifiers: chr11:g.45528111C>T (hg19) ; chr11:g.45506561C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.45506561C>T , CM000673.2:g.45506561C>T	GRCh38
NC_000011.9:g.45528111C>T , CM000673.1:g.45528111C>T	GRCh37
NC_000011.8:g.45484687C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_001748204.2:n.909-16790G>A
XR_931245.3:n.566-16790G>A