Canonical Allele Identifier: CA598511776

Gene:

Linked Data

• dbSNP Id: rs1272666826
• gnomAD v2: 11-34834179-G-A
• gnomAD v3: 11-34812632-G-A
• gnomAD v4: 11-34812632-G-A
• MyVariant Identifiers: chr11:g.34834179G>A (hg19) ; chr11:g.34812632G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.34812632G>A , CM000673.2:g.34812632G>A	GRCh38
NC_000011.9:g.34834179G>A , CM000673.1:g.34834179G>A	GRCh37
NC_000011.8:g.34790755G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_428897.2:n.579+58025G>A
XR_931188.1:n.693+58025G>A
XR_931189.1:n.854+58025G>A
XR_931190.1:n.639+58025G>A
XR_931191.1:n.689+58025G>A
XR_001748174.1:n.855+58025G>A
XR_001748176.1:n.1016+58025G>A
XR_002957246.1:n.639+58025G>A