Canonical Allele Identifier: CA2078839115
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.23722723A>T , CM000675.2:g.23722723A>T GRCh38
NC_000013.10:g.24296862A>T , CM000675.1:g.24296862A>T GRCh37
NC_000013.9:g.23194862A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_941745.1:n.370+6106A>T
XR_941746.1:n.755A>T
XR_941747.1:n.372-1306A>T
XR_941745.2:n.393+6106A>T
XR_941746.2:n.777A>T
XR_941747.2:n.394-1306A>T