Canonical Allele Identifier: CA2206404238
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.9249614A= , CM000678.2:g.9249614A= GRCh38
NC_000016.9:g.9343471A= , CM000678.1:g.9343471A= GRCh37
NC_000016.8:g.9250972A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_933054.1:n.70+64881A=