Canonical Allele Identifier: CA1608913932
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.8169717C= , CM000668.2:g.8169717C= GRCh38
NC_000006.11:g.8169950C= , CM000668.1:g.8169950C= GRCh37
NC_000006.10:g.8114949C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_926440.1:n.82+11457C=
XR_926441.1:n.189+1797C=
XR_926442.1:n.82+11457C=
XR_926443.1:n.82+11457C=
XR_001743950.1:n.179+1797C=
XR_926440.2:n.74+11457C=
XR_926441.2:n.179+1797C=
XR_926443.2:n.83+11457C=