Canonical Allele Identifier: CA1797411920
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.81478415T= , CM000670.2:g.81478415T= GRCh38
NC_000008.10:g.82390650T= , CM000670.1:g.82390650T= GRCh37
NC_000008.9:g.82553205T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001745980.1:n.514+16441T=