Canonical Allele Identifier: CA2257713069
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.35880804T= , CM000679.2:g.35880804T= GRCh38
NC_000017.9:g.31231921T= NCBI36
NG_015990.1:g.4570A=

Transcript Alleles

HGVS Amino-acid change
XR_934696.1:n.197-3578T=
XR_934697.1:n.200-3578T=
XR_001752852.1:n.426+730T=
XR_934696.2:n.91-3578T=
XR_934697.2:n.91-3578T=