Canonical Allele Identifier: CA1601790169
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.173507879T= , CM000667.2:g.173507879T= GRCh38
NC_000005.9:g.172934882T= , CM000667.1:g.172934882T= GRCh37
NC_000005.8:g.172867488T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_941238.1:n.5641+289T=
XR_941239.1:n.3602+289T=
XR_941240.1:n.5497+289T=
XR_941241.1:n.3078+289T=
XR_941242.1:n.5391+289T=
XR_941243.1:n.5568+289T=
XR_941244.1:n.2883+289T=
XR_941246.1:n.5261+289T=
XR_001743000.1:n.3529+289T=
XR_001743001.1:n.3056+289T=
XR_002956234.1:n.5200+289T=