Canonical Allele Identifier: CA15856562
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.95613139A>G , CM000677.2:g.95613139A>G GRCh38
NC_000015.9:g.96156368A>G , CM000677.1:g.96156368A>G GRCh37
NC_000015.8:g.93957372A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_932654.1:n.68+3063A>G