Canonical Allele Identifier: CA2206404193
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.9249540C= , CM000678.2:g.9249540C= GRCh38
NC_000016.9:g.9343397C= , CM000678.1:g.9343397C= GRCh37
NC_000016.8:g.9250898C= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_933054.1:n.70+64807C=