Canonical Allele Identifier: CA2293960071
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.31756492C= , CM000680.2:g.31756492C= GRCh38
NC_000018.9:g.29336455C= , CM000680.1:g.29336455C= GRCh37
NC_000018.8:g.27590453C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_935338.1:n.66-5647C=