Canonical Allele Identifier: CA1649475152
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.98047998T= , CM000668.2:g.98047998T= GRCh38
NC_000006.11:g.98495874T= , CM000668.1:g.98495874T= GRCh37
NC_000006.10:g.98602595T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_245563.2:n.372-51188T=
XR_942809.1:n.372-51188T=