HGVS | Genome Assembly |
---|---|
NC_000007.14:g.24413395T>G , CM000669.2:g.24413395T>G | GRCh38 |
NC_000007.13:g.24453014T>G , CM000669.1:g.24453014T>G | GRCh37 |
NC_000007.12:g.24419539T>G | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
XM_017012910.1:c.-89+31664A>C | XP_016868399.1:n.-89+31664A>C | |
XM_017012911.1:c.-89+31664A>C | XP_016868400.1:n.-89+31664A>C | |
XR_001745121.1:n.344+31664A>C | ||
XR_001745122.1:n.344+31664A>C | ||
XR_001745123.1:n.344+31664A>C | ||
XR_001745124.1:n.344+31664A>C | ||
XR_001745125.1:n.344+31664A>C | ||
XR_001745126.1:n.344+31664A>C | ||
XR_001745127.1:n.344+31664A>C | ||
XR_001745129.1:n.344+31664A>C | ||
XR_001745130.1:n.344+31664A>C | ||
XR_001745131.1:n.344+31664A>C | ||
XR_001745132.1:n.344+31664A>C |