Canonical Allele Identifier: CA2581219925
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.60217977A>T , CM000677.2:g.60217977A>T GRCh38
NC_000015.9:g.60510176A>T , CM000677.1:g.60510176A>T GRCh37
NC_000015.8:g.58297468A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_932310.1:n.312-34448A>T
XR_932310.2:n.609-34448A>T