HGVS | Genome Assembly |
---|---|
NC_000004.12:g.94935397T= , CM000666.2:g.94935397T= | GRCh38 |
NC_000004.11:g.95856548T= , CM000666.1:g.95856548T= | GRCh37 |
NC_000004.10:g.96075571T= | NCBI36 |
NG_009245.1:g.182421T= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000515059.6:c.-113+59497T= MANE Select | ENSP00000426617.1:n.-113+59497T= | |
ENST00000515059.5:c.-113+59497T= | ENSP00000426617.1:n.-113+59497T= | |
NM_001203.2:c.-113+59497T= | NP_001194.1:n.-113+59497T= | |
XM_011532201.1:c.-18+59497T= | XP_011530503.1:n.-18+59497T= | |
XM_011532201.2:c.-18+59497T= | XP_011530503.1:n.-18+59497T= | |
XM_017008558.1:c.-113+59497T= | XP_016864047.1:n.-113+59497T= | |
XM_017008559.1:c.-113+36347T= | XP_016864048.1:n.-113+36347T= | |
NM_001203.3:c.-113+59497T= MANE Select | NP_001194.1:n.-113+59497T= |