Canonical Allele Identifier: CA1931617879
Gene:

Linked Data

dbSNP Id: rs2041646295

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.100101717A>T , CM000672.2:g.100101717A>T GRCh38
NC_000010.10:g.101861474A>T , CM000672.1:g.101861474A>T GRCh37
NC_000010.9:g.101851464A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_946245.1:n.185+5480A>T