Canonical Allele Identifier: CA2112050697
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.94853095T= , CM000675.2:g.94853095T= GRCh38
NC_000013.10:g.95505349T= , CM000675.1:g.95505349T= GRCh37
NC_000013.9:g.94303350T= NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_110754.1:n.257-52369T=