Canonical Allele Identifier: CA1496030152
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.134601502G= , CM000666.2:g.134601502G= GRCh38
NC_000004.11:g.135522657G= , CM000666.1:g.135522657G= GRCh37
NC_000004.10:g.135742107G= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_939212.1:n.410+14143G=
XR_939214.1:n.392+14143G=
XR_939214.2:n.392+14143G=