Canonical Allele Identifier: CA1889344500
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.8697529T= , CM000672.2:g.8697529T= GRCh38
NC_000010.10:g.8739492T= , CM000672.1:g.8739492T= GRCh37
NC_000010.9:g.8779498T= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_930641.1:n.33-27728A=