Canonical Allele Identifier: CA2284269284
Gene:

Linked Data

dbSNP Id: rs1362142196

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.10382826A>G , CM000680.2:g.10382826A>G GRCh38
NC_000018.9:g.10382823A>G , CM000680.1:g.10382823A>G GRCh37
NC_000018.8:g.10372823A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_935143.1:n.919+1473A>G