Canonical Allele Identifier: CA13153189
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.44390758C>T , CM000672.2:g.44390758C>T GRCh38
NC_000010.10:g.44886206C>T , CM000672.1:g.44886206C>T GRCh37
NC_000010.9:g.44206212C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001747298.1:n.67+926C>T