Canonical Allele Identifier: CA2197752677
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.95782348T= , CM000677.2:g.95782348T= GRCh38
NC_000015.9:g.96325577T= , CM000677.1:g.96325577T= GRCh37
NC_000015.8:g.94126581T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_932654.1:n.148-42841T=