HGVS | Genome Assembly |
---|---|
NC_000022.11:g.37713077T= , CM000684.2:g.37713077T= | GRCh38 |
NC_000022.10:g.38109084T= , CM000684.1:g.38109084T= | GRCh37 |
NC_000022.9:g.36439030T= | NCBI36 |
NG_012857.1:g.21090T= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000644935.1:c.255-133T= MANE Select | ENSP00000496394.1:n.255-133T= | |
ENST00000344404.10:c.254+2511T= | ENSP00000340312.6:n.254+2511T= | |
ENST00000406386.7:c.255-133T= | ENSP00000384312.3:n.255-133T= | |
ENST00000455236.4:c.1212-133T= | ENSP00000477208.1:n.1212-133T= | |
ENST00000492485.5:n.390+2511T= | ||
NM_001039141.2:c.255-133T= | NP_001034230.1:n.255-133T= | |
NM_001039141.3:c.255-133T= MANE Select | NP_001034230.1:n.255-133T= |