Canonical Allele Identifier: CA2269954689
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.63506444T= , CM000679.2:g.63506444T= GRCh38
NC_000017.10:g.61583805T= , CM000679.1:g.61583805T= GRCh37
NC_000017.9:g.58937537T= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000577647.2:c.1970-612T= ENSP00000464149.1:n.1970-612T=