HGVS | Genome Assembly |
---|---|
NC_000010.11:g.94974432T>C , CM000672.2:g.94974432T>C | GRCh38 |
NC_000010.10:g.96734189T>C , CM000672.1:g.96734189T>C | GRCh37 |
NC_000010.9:g.96724179T>C | NCBI36 |
NG_008385.1:g.40775T>C | |
NG_008385.2:g.41275T>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000260682.8:c.961+2187T>C MANE Select | ENSP00000260682.6:n.961+2187T>C | |
ENST00000643112.1:c.820-6751T>C | ENSP00000496202.1:n.820-6751T>C | |
ENST00000260682.6:c.961+2187T>C | ENSP00000260682.6:n.961+2187T>C | |
NM_000771.3:c.961+2187T>C | NP_000762.2:n.961+2187T>C | |
NM_000771.4:c.961+2187T>C MANE Select | NP_000762.2:n.961+2187T>C |