Canonical Allele Identifier: CA2293960188
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.31756769C= , CM000680.2:g.31756769C= GRCh38
NC_000018.9:g.29336732C= , CM000680.1:g.29336732C= GRCh37
NC_000018.8:g.27590730C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_935338.1:n.66-5370C=