Canonical Allele Identifier: CA2500404168
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.49645820T>C , CM000680.2:g.49645820T>C GRCh38
NC_000018.9:g.47172190T>C , CM000680.1:g.47172190T>C GRCh37
NC_000018.8:g.45426188T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_935461.1:n.162-16214T>C
XR_001753446.1:n.898-16214T>C