Canonical Allele Identifier: CA2136398847
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.50856846C= , CM000676.2:g.50856846C= GRCh38
NC_000014.8:g.51323564C= , CM000676.1:g.51323564C= GRCh37
NC_000014.7:g.50393314C= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_943848.1:n.282+1252G=
XR_943848.2:n.643+1252G=