Canonical Allele Identifier: CA2800209036
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.94853053C>G , CM000675.2:g.94853053C>G GRCh38
NC_000013.10:g.95505307C>G , CM000675.1:g.95505307C>G GRCh37
NC_000013.9:g.94303308C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_110754.1:n.257-52411C>G