Canonical Allele Identifier: CA184586763
Gene:

Identifiers and link-outs to other resources

dbSNP Id: rs10088262

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.123753462A>G , CM000670.2:g.123753462A>G GRCh38
NC_000008.10:g.124765702A>G , CM000670.1:g.124765702A>G GRCh37
NC_000008.9:g.124834883A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_928607.1:n.153-11321A>G
XR_928607.3:n.324-11321A>G