Canonical Allele Identifier: CA2112050471
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.94852983A= , CM000675.2:g.94852983A= GRCh38
NC_000013.10:g.95505237A= , CM000675.1:g.95505237A= GRCh37
NC_000013.9:g.94303238A= NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_110754.1:n.257-52481A=