HGVS | Genome Assembly |
---|---|
NC_000022.11:g.37710701C= , CM000684.2:g.37710701C= | GRCh38 |
NC_000022.10:g.38106708C= , CM000684.1:g.38106708C= | GRCh37 |
NC_000022.9:g.36436654C= | NCBI36 |
NG_012857.1:g.18714C= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000644935.1:c.254+135C= MANE Select | ENSP00000496394.1:n.254+135C= | |
ENST00000344404.10:c.254+135C= | ENSP00000340312.6:n.254+135C= | |
ENST00000406386.7:c.254+135C= | ENSP00000384312.3:n.254+135C= | |
ENST00000455236.4:c.1211+135C= | ENSP00000477208.1:n.1211+135C= | |
ENST00000492485.5:n.390+135C= | ||
NM_001039141.2:c.254+135C= | NP_001034230.1:n.254+135C= | |
NM_001039141.3:c.254+135C= MANE Select | NP_001034230.1:n.254+135C= |