Canonical Allele Identifier: CA673239447

Gene:

Linked Data

• dbSNP Id: rs1414359166
• gnomAD v3: 11-128455657-A-G
• gnomAD v4: 11-128455657-A-G
• MyVariant Identifiers: chr11:g.128325552A>G (hg19) ; chr11:g.128455657A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.128455657A>G , CM000673.2:g.128455657A>G	GRCh38
NC_000011.9:g.128325552A>G , CM000673.1:g.128325552A>G	GRCh37
NC_000011.8:g.127830762A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_948164.1:n.4377A>G
XR_948165.1:n.3467+910A>G