HGVS | Genome Assembly |
---|---|
NC_000016.10:g.11597836A>G , CM000678.2:g.11597836A>G | GRCh38 |
NC_000016.9:g.11691692A>G , CM000678.1:g.11691692A>G | GRCh37 |
NC_000016.8:g.11599193A>G | NCBI36 |
HGVS | Amino-acid change | |
---|---|---|
ENST00000571627.5:c.-6+552T>C | ENSP00000460743.1:n.-6+552T>C | |
ENST00000574848.5:c.85+35697T>C | ENSP00000459898.1:n.85+35697T>C | |
ENST00000576036.5:c.-6+31287T>C | ENSP00000461667.1:n.-6+31287T>C | |
ENST00000576334.1:c.85+35697T>C | ENSP00000458538.1:n.85+35697T>C | |
XM_011522754.1:c.85+35697T>C | XP_011521056.1:n.85+35697T>C | |
XM_011522754.3:c.85+35697T>C | XP_011521056.1:n.85+35697T>C | |
XM_017023896.1:c.-6+31287T>C | XP_016879385.1:n.-6+31287T>C |