Canonical Allele Identifier: CA674857342

Gene:

Linked Data

• dbSNP Id: rs1298825646
• gnomAD v3: 11-2444545-G-A
• gnomAD v4: 11-2444545-G-A
• MyVariant Identifiers: chr11:g.2465775G>A (hg19) ; chr11:g.2444545G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.2444545G>A , CM000673.2:g.2444545G>A	GRCh38
NC_000011.9:g.2465775G>A , CM000673.1:g.2465775G>A	GRCh37
NC_000011.8:g.2422351G>A	NCBI36
NG_008935.1:g.4555G>A , LRG_287:g.4555G>A

Transcript Alleles

HGVS	Amino-acid Change
XR_930984.1:n.26C>T