Canonical Allele Identifier: CA2302316775
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.49645833C= , CM000680.2:g.49645833C= GRCh38
NC_000018.9:g.47172203C= , CM000680.1:g.47172203C= GRCh37
NC_000018.8:g.45426201C= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_935461.1:n.162-16201C=
XR_001753446.1:n.898-16201C=