Canonical Allele Identifier: CA2206404268
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.9249677C= , CM000678.2:g.9249677C= GRCh38
NC_000016.9:g.9343534C= , CM000678.1:g.9343534C= GRCh37
NC_000016.8:g.9251035C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_933054.1:n.70+64944C=