Canonical Allele Identifier: CA2112050627
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.94853060T= , CM000675.2:g.94853060T= GRCh38
NC_000013.10:g.95505314T= , CM000675.1:g.95505314T= GRCh37
NC_000013.9:g.94303315T= NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_110754.1:n.257-52404T=