Canonical Allele Identifier: CA2269954674
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.63506403T= , CM000679.2:g.63506403T= GRCh38
NC_000017.10:g.61583764T= , CM000679.1:g.61583764T= GRCh37
NC_000017.9:g.58937496T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000577647.2:c.1970-653T= ENSP00000464149.1:n.1970-653T=