Canonical Allele Identifier: CA2284269344
Gene:

Linked Data

dbSNP Id: rs1969409603

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.10382945C>A , CM000680.2:g.10382945C>A GRCh38
NC_000018.9:g.10382942C>A , CM000680.1:g.10382942C>A GRCh37
NC_000018.8:g.10372942C>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_935143.1:n.919+1592C>A