Canonical Allele Identifier: CA1888525189
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.7047089G= , CM000672.2:g.7047089G= GRCh38
NC_000010.10:g.7089051G= , CM000672.1:g.7089051G= GRCh37
NC_000010.9:g.7129057G= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_930623.1:n.173-16772C=
XR_930624.1:n.171-16772C=
XR_930625.1:n.172-16772C=
XR_930626.1:n.168-16772C=
XR_930627.1:n.173-16772C=
XR_001747351.1:n.364-16772C=
XR_001747352.1:n.364-16772C=
XR_001747353.1:n.188-34433C=
XR_001747354.1:n.364-16772C=
XR_930623.2:n.364-16772C=
XR_930624.2:n.364-16772C=
XR_930625.2:n.364-16772C=
XR_930626.2:n.364-16772C=
XR_930627.2:n.364-16772C=