Canonical Allele Identifier: CA2293960204
Gene:

Linked Data

dbSNP Id: rs2031434286

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.31756805G>T , CM000680.2:g.31756805G>T GRCh38
NC_000018.9:g.29336768G>T , CM000680.1:g.29336768G>T GRCh37
NC_000018.8:g.27590766G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_935338.1:n.66-5334G>T