Canonical Allele Identifier: CA2293960310
Gene:

Linked Data

dbSNP Id: rs2031436966

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.31757032T>C , CM000680.2:g.31757032T>C GRCh38
NC_000018.9:g.29336995T>C , CM000680.1:g.29336995T>C GRCh37
NC_000018.8:g.27590993T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_935338.1:n.66-5107T>C