Canonical Allele Identifier: CA2112050664
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.94853081C= , CM000675.2:g.94853081C= GRCh38
NC_000013.10:g.95505335C= , CM000675.1:g.95505335C= GRCh37
NC_000013.9:g.94303336C= NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_110754.1:n.257-52383C=