Canonical Allele Identifier: CA2206404252
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.9249639A= , CM000678.2:g.9249639A= GRCh38
NC_000016.9:g.9343496A= , CM000678.1:g.9343496A= GRCh37
NC_000016.8:g.9250997A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_933054.1:n.70+64906A=