Canonical Allele Identifier: CA2138937531
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.56419968A= , CM000676.2:g.56419968A= GRCh38
NC_000014.8:g.56886686A= , CM000676.1:g.56886686A= GRCh37
NC_000014.7:g.55956439A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_943903.1:n.202-6220A=