Canonical Allele Identifier: CA1899263529
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.30201822A= , CM000672.2:g.30201822A= GRCh38
NC_000010.10:g.30490751A= , CM000672.1:g.30490751A= GRCh37
NC_000010.9:g.30530757A= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_930791.1:n.1193-1665A=
XR_930791.2:n.1449-1665A=