Canonical Allele Identifier: CA222002628

Gene:

Linked Data

• dbSNP Id: rs77082331
• gnomAD v2: 11-45528150-A-G
• gnomAD v3: 11-45506600-A-G
• gnomAD v4: 11-45506600-A-G
• MyVariant Identifiers: chr11:g.45528150A>G (hg19) ; chr11:g.45506600A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.45506600A>G , CM000673.2:g.45506600A>G	GRCh38
NC_000011.9:g.45528150A>G , CM000673.1:g.45528150A>G	GRCh37
NC_000011.8:g.45484726A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_001748204.2:n.909-16829T>C
XR_931245.3:n.566-16829T>C