HGVS | Genome Assembly |
---|---|
NC_000023.11:g.101348089A= , CM000685.2:g.101348089A= | GRCh38 |
NC_000023.10:g.100603077A= , CM000685.1:g.100603077A= | GRCh37 |
NC_000023.9:g.100489733A= | NCBI36 |
NG_009616.1:g.43136T= , LRG_128:g.43136T= | |
NG_011734.1:g.5881T= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000372902.4:c.132+444T= MANE Select | ENSP00000361993.3:n.132+444T= | |
ENST00000644112.2:c.*298T= | ENSP00000494385.1:n.*298T= | |
ENST00000645279.1:c.*298T= | ENSP00000494239.1:n.*298T= | |
ENST00000647480.1:n.487T= | ||
ENST00000372902.3:c.132+444T= | ENSP00000361993.3:n.132+444T= | |
ENST00000480575.1:n.530T= | ||
NM_001145951.1:c.*298T= | NP_001139423.1:n.*298T= | |
NM_004085.3:c.132+444T= | NP_004076.1:n.132+444T= | |
NM_004085.4:c.132+444T= MANE Select | NP_004076.1:n.132+444T= | |
NM_001145951.2:c.*298T= | NP_001139423.1:n.*298T= |