Canonical Allele Identifier: CA2136398934
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.50857036G= , CM000676.2:g.50857036G= GRCh38
NC_000014.8:g.51323754G= , CM000676.1:g.51323754G= GRCh37
NC_000014.7:g.50393504G= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_943848.1:n.282+1062C=
XR_943848.2:n.643+1062C=