Canonical Allele Identifier: CA2112050660
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.94853078T= , CM000675.2:g.94853078T= GRCh38
NC_000013.10:g.95505332T= , CM000675.1:g.95505332T= GRCh37
NC_000013.9:g.94303333T= NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_110754.1:n.257-52386T=