Canonical Allele Identifier: CA220643998

Gene:

Linked Data

• dbSNP Id: rs1023100079
• gnomAD v2: 11-34834168-G-A
• gnomAD v3: 11-34812621-G-A
• gnomAD v4: 11-34812621-G-A
• MyVariant Identifiers: chr11:g.34834168G>A (hg19) ; chr11:g.34812621G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.34812621G>A , CM000673.2:g.34812621G>A	GRCh38
NC_000011.9:g.34834168G>A , CM000673.1:g.34834168G>A	GRCh37
NC_000011.8:g.34790744G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_428897.2:n.579+58014G>A
XR_931188.1:n.693+58014G>A
XR_931189.1:n.854+58014G>A
XR_931190.1:n.639+58014G>A
XR_931191.1:n.689+58014G>A
XR_001748174.1:n.855+58014G>A
XR_001748176.1:n.1016+58014G>A
XR_002957246.1:n.639+58014G>A