Canonical Allele Identifier: CA14517179
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.49655298A>T , CM000680.2:g.49655298A>T GRCh38
NC_000018.9:g.47181668A>T , CM000680.1:g.47181668A>T GRCh37
NC_000018.8:g.45435666A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_935461.1:n.162-6736A>T
XR_001753446.1:n.898-6736A>T