Canonical Allele Identifier: CA2302316787
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.49645854C= , CM000680.2:g.49645854C= GRCh38
NC_000018.9:g.47172224C= , CM000680.1:g.47172224C= GRCh37
NC_000018.8:g.45426222C= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_935461.1:n.162-16180C=
XR_001753446.1:n.898-16180C=