Canonical Allele Identifier: CA2293960303
Gene:

Linked Data

dbSNP Id: rs2031436853

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.31757023A>T , CM000680.2:g.31757023A>T GRCh38
NC_000018.9:g.29336986A>T , CM000680.1:g.29336986A>T GRCh37
NC_000018.8:g.27590984A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_935338.1:n.66-5116A>T