Canonical Allele Identifier: CA1496030102
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.134601422A= , CM000666.2:g.134601422A= GRCh38
NC_000004.11:g.135522577A= , CM000666.1:g.135522577A= GRCh37
NC_000004.10:g.135742027A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_939212.1:n.410+14063A=
XR_939214.1:n.392+14063A=
XR_939214.2:n.392+14063A=