Canonical Allele Identifier: CA2199721360
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.99817302A= , CM000677.2:g.99817302A= GRCh38
NC_000015.9:g.100357507A= , CM000677.1:g.100357507A= GRCh37
NC_000015.8:g.98175030A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_932717.1:n.408+4216A=
XR_932718.1:n.408+4216A=
XR_932719.1:n.514+9000A=
XR_932720.1:n.409-1636A=
NR_135737.1:n.346+4216A=