Canonical Allele Identifier: CA2284239378
Gene:

Linked Data

dbSNP Id: rs1968769271

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.10321311C>T , CM000680.2:g.10321311C>T GRCh38
NC_000018.9:g.10321308C>T , CM000680.1:g.10321308C>T GRCh37
NC_000018.8:g.10311308C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_935138.1:n.665+837G>A
XR_001753344.1:n.650+837G>A
XR_001753345.1:n.810G>A
XR_001753346.1:n.549+837G>A