HGVS | Genome Assembly |
---|---|
NC_000002.12:g.216028995T= , CM000664.2:g.216028995T= | GRCh38 |
NC_000002.11:g.216893718T= , CM000664.1:g.216893718T= | GRCh37 |
NC_000002.10:g.216601963T= | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000420348.1:c.-68+3794A= (MREG) | ENSP00000404470.1:n.-68+3794A= | |
ENST00000424992.5:c.-68+4967A= (MREG) | ENSP00000413302.1:n.-68+4967A= | |
ENST00000439791.5:c.-68+4688A= (MREG) | ENSP00000411076.1:n.-68+4688A= | |
ENST00000442122.5:c.*440+10196A= (PECR) | ENSP00000395512.1:n.*440+10196A= | |
NM_001372189.1:c.-68+4967A= (MREG) | NP_001359118.1:n.-68+4967A= | |
NM_001372190.1:c.-68+4688A= (MREG) | NP_001359119.1:n.-68+4688A= |