Canonical Allele Identifier: CA230077626

Gene:

Linked Data

• dbSNP Id: rs979464403
• gnomAD v3: 11-116442626-G-A
• gnomAD v4: 11-116442626-G-A
• MyVariant Identifiers: chr11:g.116313343G>A (hg19) ; chr11:g.116442626G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.116442626G>A , CM000673.2:g.116442626G>A	GRCh38
NC_000011.9:g.116313343G>A , CM000673.1:g.116313343G>A	GRCh37
NC_000011.8:g.115818553G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_001748403.1:n.349+31251C>T