Canonical Allele Identifier: CA2805806093
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.9249674C>T , CM000678.2:g.9249674C>T GRCh38
NC_000016.9:g.9343531C>T , CM000678.1:g.9343531C>T GRCh37
NC_000016.8:g.9251032C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_933054.1:n.70+64941C>T