Canonical Allele Identifier: CA1694961302
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.24413292G= , CM000669.2:g.24413292G= GRCh38
NC_000007.13:g.24452911G= , CM000669.1:g.24452911G= GRCh37
NC_000007.12:g.24419436G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XM_017012910.1:c.-89+31767C= XP_016868399.1:n.-89+31767C=
XM_017012911.1:c.-89+31767C= XP_016868400.1:n.-89+31767C=
XR_001745121.1:n.344+31767C=
XR_001745122.1:n.344+31767C=
XR_001745123.1:n.344+31767C=
XR_001745124.1:n.344+31767C=
XR_001745125.1:n.344+31767C=
XR_001745126.1:n.344+31767C=
XR_001745127.1:n.344+31767C=
XR_001745129.1:n.344+31767C=
XR_001745130.1:n.344+31767C=
XR_001745131.1:n.344+31767C=
XR_001745132.1:n.344+31767C=