Canonical Allele Identifier: CA2206404239
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.9249615C= , CM000678.2:g.9249615C= GRCh38
NC_000016.9:g.9343472C= , CM000678.1:g.9343472C= GRCh37
NC_000016.8:g.9250973C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_933054.1:n.70+64882C=