Canonical Allele Identifier: CA2112050673
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.94853091A= , CM000675.2:g.94853091A= GRCh38
NC_000013.10:g.95505345A= , CM000675.1:g.95505345A= GRCh37
NC_000013.9:g.94303346A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_110754.1:n.257-52373A=