Canonical Allele Identifier: CA2293960155
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.31756681C= , CM000680.2:g.31756681C= GRCh38
NC_000018.9:g.29336644C= , CM000680.1:g.29336644C= GRCh37
NC_000018.8:g.27590642C= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_935338.1:n.66-5458C=