HGVS | Genome Assembly |
---|---|
NC_000004.12:g.94935416G= , CM000666.2:g.94935416G= | GRCh38 |
NC_000004.11:g.95856567G= , CM000666.1:g.95856567G= | GRCh37 |
NC_000004.10:g.96075590G= | NCBI36 |
NG_009245.1:g.182440G= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000515059.6:c.-113+59516G= MANE Select | ENSP00000426617.1:n.-113+59516G= | |
ENST00000515059.5:c.-113+59516G= | ENSP00000426617.1:n.-113+59516G= | |
NM_001203.2:c.-113+59516G= | NP_001194.1:n.-113+59516G= | |
XM_011532201.1:c.-18+59516G= | XP_011530503.1:n.-18+59516G= | |
XM_011532201.2:c.-18+59516G= | XP_011530503.1:n.-18+59516G= | |
XM_017008558.1:c.-113+59516G= | XP_016864047.1:n.-113+59516G= | |
XM_017008559.1:c.-113+36366G= | XP_016864048.1:n.-113+36366G= | |
NM_001203.3:c.-113+59516G= MANE Select | NP_001194.1:n.-113+59516G= |