Canonical Allele Identifier: CA1886690292
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.3366809A= , CM000672.2:g.3366809A= GRCh38
NC_000010.10:g.3409001A= , CM000672.1:g.3409001A= GRCh37
NC_000010.9:g.3399001A= NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_131187.1:n.162+47953A=