Canonical Allele Identifier: CA1796404035
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.79191050T= , CM000670.2:g.79191050T= GRCh38
NC_000008.10:g.80103285T= , CM000670.1:g.80103285T= GRCh37
NC_000008.9:g.80265840T= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_001745720.1:n.105+679T=