Canonical Allele Identifier: CA2002576342
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.116442691A= , CM000673.2:g.116442691A= GRCh38
NC_000011.9:g.116313408A= , CM000673.1:g.116313408A= GRCh37
NC_000011.8:g.115818618A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001748403.1:n.349+31186T=