Canonical Allele Identifier: CA1818149687
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.126999664T= , CM000670.2:g.126999664T= GRCh38
NC_000008.10:g.128011909T= , CM000670.1:g.128011909T= GRCh37
NC_000008.9:g.128081091T= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_001746076.2:n.1301-6891T=