Canonical Allele Identifier: CA1886690274
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.3366770T= , CM000672.2:g.3366770T= GRCh38
NC_000010.10:g.3408962T= , CM000672.1:g.3408962T= GRCh37
NC_000010.9:g.3398962T= NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_131187.1:n.162+47914T=