Canonical Allele Identifier: CA220638161

Gene:

Linked Data

• dbSNP Id: rs1045920675
• gnomAD v3: 11-34759365-A-G
• gnomAD v4: 11-34759365-A-G
• MyVariant Identifiers: chr11:g.34780912A>G (hg19) ; chr11:g.34759365A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.34759365A>G , CM000673.2:g.34759365A>G	GRCh38
NC_000011.9:g.34780912A>G , CM000673.1:g.34780912A>G	GRCh37
NC_000011.8:g.34737488A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_428897.2:n.579+4758A>G
XR_931188.1:n.693+4758A>G
XR_931189.1:n.854+4758A>G
XR_931190.1:n.639+4758A>G
XR_931191.1:n.689+4758A>G
XR_001748174.1:n.855+4758A>G
XR_001748176.1:n.1016+4758A>G
XR_002957246.1:n.639+4758A>G