Canonical Allele Identifier: CA2197752691
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.95782368C= , CM000677.2:g.95782368C= GRCh38
NC_000015.9:g.96325597C= , CM000677.1:g.96325597C= GRCh37
NC_000015.8:g.94126601C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_932654.1:n.148-42821C=