Canonical Allele Identifier: CA1886690282
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.3366792A= , CM000672.2:g.3366792A= GRCh38
NC_000010.10:g.3408984A= , CM000672.1:g.3408984A= GRCh37
NC_000010.9:g.3398984A= NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_131187.1:n.162+47936A=