Canonical Allele Identifier: CA2193585410
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.87152185T= , CM000677.2:g.87152185T= GRCh38
NC_000015.9:g.87695416T= , CM000677.1:g.87695416T= GRCh37
NC_000015.8:g.85496420T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_932582.1:n.167-26042T=
XR_932582.2:n.167-26042T=