Canonical Allele Identifier: CA1796404079
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.79191159T= , CM000670.2:g.79191159T= GRCh38
NC_000008.10:g.80103394T= , CM000670.1:g.80103394T= GRCh37
NC_000008.9:g.80265949T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001745720.1:n.105+788T=