Canonical Allele Identifier: CA2293960130
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.31756628A= , CM000680.2:g.31756628A= GRCh38
NC_000018.9:g.29336591A= , CM000680.1:g.29336591A= GRCh37
NC_000018.8:g.27590589A= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_935338.1:n.66-5511A=