Canonical Allele Identifier: CA2293960113
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.31756587G= , CM000680.2:g.31756587G= GRCh38
NC_000018.9:g.29336550G= , CM000680.1:g.29336550G= GRCh37
NC_000018.8:g.27590548G= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_935338.1:n.66-5552G=