Canonical Allele Identifier: CA1694961258
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.24413196T= , CM000669.2:g.24413196T= GRCh38
NC_000007.13:g.24452815T= , CM000669.1:g.24452815T= GRCh37
NC_000007.12:g.24419340T= NCBI36

Transcript Alleles

HGVS Amino-acid change
XM_017012910.1:c.-89+31863A= XP_016868399.1:n.-89+31863A=
XM_017012911.1:c.-89+31863A= XP_016868400.1:n.-89+31863A=
XR_001745121.1:n.344+31863A=
XR_001745122.1:n.344+31863A=
XR_001745123.1:n.344+31863A=
XR_001745124.1:n.344+31863A=
XR_001745125.1:n.344+31863A=
XR_001745126.1:n.344+31863A=
XR_001745127.1:n.344+31863A=
XR_001745129.1:n.344+31863A=
XR_001745130.1:n.344+31863A=
XR_001745131.1:n.344+31863A=
XR_001745132.1:n.344+31863A=