Canonical Allele Identifier: CA2293960077
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.31756506C= , CM000680.2:g.31756506C= GRCh38
NC_000018.9:g.29336469C= , CM000680.1:g.29336469C= GRCh37
NC_000018.8:g.27590467C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_935338.1:n.66-5633C=