Canonical Allele Identifier: CA2809771338
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.50211619G>T , CM000679.2:g.50211619G>T GRCh38
NC_000017.10:g.48288980G>T , CM000679.1:g.48288980G>T GRCh37
NC_000017.9:g.45643979G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_934838.1:n.42+2213G>T