Canonical Allele Identifier: CA602555874

Gene:

Linked Data

• dbSNP Id: rs1356798911
• gnomAD v2: 11-128325452-A-G
• gnomAD v3: 11-128455557-A-G
• gnomAD v4: 11-128455557-A-G
• MyVariant Identifiers: chr11:g.128325452A>G (hg19) ; chr11:g.128455557A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.128455557A>G , CM000673.2:g.128455557A>G	GRCh38
NC_000011.9:g.128325452A>G , CM000673.1:g.128325452A>G	GRCh37
NC_000011.8:g.127830662A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_948164.1:n.4277A>G
XR_948165.1:n.3467+810A>G