Canonical Allele Identifier: CA602555873

Gene:

Linked Data

• dbSNP Id: rs1327377375
• gnomAD v2: 11-128325437-C-G
• gnomAD v3: 11-128455542-C-G
• gnomAD v4: 11-128455542-C-G
• MyVariant Identifiers: chr11:g.128325437C>G (hg19) ; chr11:g.128455542C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.128455542C>G , CM000673.2:g.128455542C>G	GRCh38
NC_000011.9:g.128325437C>G , CM000673.1:g.128325437C>G	GRCh37
NC_000011.8:g.127830647C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_948164.1:n.4262C>G
XR_948165.1:n.3467+795C>G