Canonical Allele Identifier: CA2284269267
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.10382791T= , CM000680.2:g.10382791T= GRCh38
NC_000018.9:g.10382788T= , CM000680.1:g.10382788T= GRCh37
NC_000018.8:g.10372788T= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_935143.1:n.919+1438T=