HGVS | Genome Assembly |
---|---|
NC_000014.9:g.74259784T>G , CM000676.2:g.74259784T>G | GRCh38 |
NC_000014.8:g.74726487T>G , CM000676.1:g.74726487T>G | GRCh37 |
NC_000014.7:g.73796240T>G | NCBI36 |
NG_013092.1:g.25313T>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000261980.3:c.760+2T>G MANE Select | ENSP00000261980.2:n.760+2T>G | |
ENST00000261980.2:c.760+2T>G | ENSP00000261980.2:n.760+2T>G | |
NM_182894.2:c.760+2T>G | NP_878314.1:n.760+2T>G | |
XM_011536719.1:c.760+2T>G | XP_011535021.1:n.760+2T>G | |
NM_182894.3:c.760+2T>G MANE Select | NP_878314.1:n.760+2T>G |