Canonical Allele Identifier: CA1898741261
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.29075705T= , CM000672.2:g.29075705T= GRCh38
NC_000010.10:g.29364634T= , CM000672.1:g.29364634T= GRCh37
NC_000010.9:g.29404640T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001747284.1:n.127-3787T=