Canonical Allele Identifier: CA2206404143
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.9249441T= , CM000678.2:g.9249441T= GRCh38
NC_000016.9:g.9343298T= , CM000678.1:g.9343298T= GRCh37
NC_000016.8:g.9250799T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_933054.1:n.70+64708T=