Canonical Allele Identifier: CA1143572982
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.224068619A= , CM000663.2:g.224068619A= GRCh38
NC_000001.10:g.224256321A= , CM000663.1:g.224256321A= GRCh37
NC_000001.9:g.222322944A= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_949173.1:n.385+965A=
XR_001737824.1:n.242+965A=