Canonical Allele Identifier: CA242665987
Gene:

Identifiers and link-outs to other resources

dbSNP Id: rs11111285

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.102501478A>G , CM000674.2:g.102501478A>G GRCh38
NC_000012.11:g.102895256A>G , CM000674.1:g.102895256A>G GRCh37
NC_000012.10:g.101419386A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_001749289.1:n.1952+17590A>G