Canonical Allele Identifier: CA1223909890
Gene:

Linked Data

dbSNP Id: rs1655906653

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.224068542A>G , CM000663.2:g.224068542A>G GRCh38
NC_000001.10:g.224256244A>G , CM000663.1:g.224256244A>G GRCh37
NC_000001.9:g.222322867A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_949173.1:n.385+888A>G
XR_001737824.1:n.242+888A>G