Canonical Allele Identifier: CA2552811012
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.134601436A>T , CM000666.2:g.134601436A>T GRCh38
NC_000004.11:g.135522591A>T , CM000666.1:g.135522591A>T GRCh37
NC_000004.10:g.135742041A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_939212.1:n.410+14077A>T
XR_939214.1:n.392+14077A>T
XR_939214.2:n.392+14077A>T