Canonical Allele Identifier: CA1496030160
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.134601528T= , CM000666.2:g.134601528T= GRCh38
NC_000004.11:g.135522683T= , CM000666.1:g.135522683T= GRCh37
NC_000004.10:g.135742133T= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_939212.1:n.410+14169T=
XR_939214.1:n.392+14169T=
XR_939214.2:n.392+14169T=