HGVS | Genome Assembly |
---|---|
NC_000022.11:g.37713175T= , CM000684.2:g.37713175T= | GRCh38 |
NC_000022.10:g.38109182T= , CM000684.1:g.38109182T= | GRCh37 |
NC_000022.9:g.36439128T= | NCBI36 |
NG_012857.1:g.21188T= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000644935.1:c.255-35T= MANE Select | ENSP00000496394.1:n.255-35T= | |
ENST00000344404.10:c.255-2588T= | ENSP00000340312.6:n.255-2588T= | |
ENST00000406386.7:c.255-35T= | ENSP00000384312.3:n.255-35T= | |
ENST00000455236.4:c.1212-35T= | ENSP00000477208.1:n.1212-35T= | |
ENST00000492485.5:n.391-2588T= | ||
NM_001039141.2:c.255-35T= | NP_001034230.1:n.255-35T= | |
NM_001039141.3:c.255-35T= MANE Select | NP_001034230.1:n.255-35T= |