HGVS | Genome Assembly |
---|---|
NC_000007.14:g.94404582T= , CM000669.2:g.94404582T= | GRCh38 |
NC_000007.13:g.94033894T= , CM000669.1:g.94033894T= | GRCh37 |
NC_000007.12:g.93871830T= | NCBI36 |
NG_007405.1:g.15022T= , LRG_2:g.15022T= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000297268.11:c.306T= MANE Select | ENSP00000297268.6:p.Pro102= | |
ENST00000297268.10:c.306T= | ENSP00000297268.6:p.Pro102= | |
ENST00000620463.1:c.300T= | ENSP00000477719.1:p.Pro100= | |
NM_000089.3:c.306T= , LRG_2t1:c.306T= | NP_000080.2:p.Pro102= | |
NM_000089.4:c.306T= MANE Select | NP_000080.2:p.Pro102= |