Canonical Allele Identifier: CA2284269291
Gene:

Linked Data

dbSNP Id: rs1969408522

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.10382835C>A , CM000680.2:g.10382835C>A GRCh38
NC_000018.9:g.10382832C>A , CM000680.1:g.10382832C>A GRCh37
NC_000018.8:g.10372832C>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_935143.1:n.919+1482C>A