Canonical Allele Identifier: CA2580925569
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.29075768G>T , CM000672.2:g.29075768G>T GRCh38
NC_000010.10:g.29364697G>T , CM000672.1:g.29364697G>T GRCh37
NC_000010.9:g.29404703G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001747284.1:n.127-3724G>T