Canonical Allele Identifier: CA2141801281
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.62501780T= , CM000676.2:g.62501780T= GRCh38
NC_000014.8:g.62968498T= , CM000676.1:g.62968498T= GRCh37
NC_000014.7:g.62038251T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_943932.1:n.116-2261T=
XR_943932.2:n.103-2261T=