HGVS | Genome Assembly |
---|---|
NC_000010.11:g.94981303T>C , CM000672.2:g.94981303T>C | GRCh38 |
NC_000010.10:g.96741060T>C , CM000672.1:g.96741060T>C | GRCh37 |
NC_000010.9:g.96731050T>C | NCBI36 |
NG_008385.1:g.47646T>C | |
NG_008385.2:g.48146T>C |
HGVS | Amino-acid change | |
---|---|---|
ENST00000260682.8:c.1082T>C MANE Select | ENSP00000260682.6:p.Leu361Pro | |
ENST00000643112.1:c.*91T>C | ENSP00000496202.1:n.*91T>C | |
ENST00000260682.6:c.1082T>C | ENSP00000260682.6:p.Leu361Pro | |
NM_000771.3:c.1082T>C | NP_000762.2:p.Leu361Pro | |
NM_000771.4:c.1082T>C MANE Select | NP_000762.2:p.Leu361Pro |