Canonical Allele Identifier: CA2199721345
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.99817286A= , CM000677.2:g.99817286A= GRCh38
NC_000015.9:g.100357491A= , CM000677.1:g.100357491A= GRCh37
NC_000015.8:g.98175014A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_932717.1:n.408+4200A=
XR_932718.1:n.408+4200A=
XR_932719.1:n.514+8984A=
XR_932720.1:n.409-1652A=
NR_135737.1:n.346+4200A=