Canonical Allele Identifier: CA602119349

Gene:

Linked Data

• dbSNP Id: rs1295134041
• gnomAD v2: 11-116313411-A-G
• gnomAD v3: 11-116442694-A-G
• gnomAD v4: 11-116442694-A-G
• MyVariant Identifiers: chr11:g.116313411A>G (hg19) ; chr11:g.116442694A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.116442694A>G , CM000673.2:g.116442694A>G	GRCh38
NC_000011.9:g.116313411A>G , CM000673.1:g.116313411A>G	GRCh37
NC_000011.8:g.115818621A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_001748403.1:n.349+31183T>C