Canonical Allele Identifier: CA216292240

Gene:

Linked Data

• dbSNP Id: rs983650814
• MyVariant Identifiers: chr11:g.2465788G>C (hg19) ; chr11:g.2444558G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.2444558G>C , CM000673.2:g.2444558G>C	GRCh38
NC_000011.9:g.2465788G>C , CM000673.1:g.2465788G>C	GRCh37
NC_000011.8:g.2422364G>C	NCBI36
NG_008935.1:g.4568G>C , LRG_287:g.4568G>C

Transcript Alleles

HGVS	Amino-acid Change
XR_930984.1:n.13C>G