Canonical Allele Identifier: CA2782088788
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.125478735C>T , CM000670.2:g.125478735C>T GRCh38
NC_000008.10:g.126490977C>T , CM000670.1:g.126490977C>T GRCh37
NC_000008.9:g.126560159C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_928628.1:n.256+5421C>T