Canonical Allele Identifier: CA2136398907
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.50856981C= , CM000676.2:g.50856981C= GRCh38
NC_000014.8:g.51323699C= , CM000676.1:g.51323699C= GRCh37
NC_000014.7:g.50393449C= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_943848.1:n.282+1117G=
XR_943848.2:n.643+1117G=