Canonical Allele Identifier: CA16513436
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.93493459A>G , CM000677.2:g.93493459A>G GRCh38
NC_000015.9:g.94036688A>G , CM000677.1:g.94036688A>G GRCh37
NC_000015.8:g.91837692A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_932628.1:n.306-36778A>G
XR_001751669.1:n.306-2775A>G
XR_001751670.1:n.448-2775A>G
XR_001751671.1:n.499-36778A>G