Canonical Allele Identifier: CA1608913979
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.8169766T= , CM000668.2:g.8169766T= GRCh38
NC_000006.11:g.8169999T= , CM000668.1:g.8169999T= GRCh37
NC_000006.10:g.8114998T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_926440.1:n.82+11506T=
XR_926441.1:n.189+1846T=
XR_926442.1:n.82+11506T=
XR_926443.1:n.82+11506T=
XR_001743950.1:n.179+1846T=
XR_926440.2:n.74+11506T=
XR_926441.2:n.179+1846T=
XR_926443.2:n.83+11506T=