HGVS | Genome Assembly |
---|---|
NC_000011.10:g.68036619T= , CM000673.2:g.68036619T= | GRCh38 |
NC_000011.9:g.67804086T= , CM000673.1:g.67804086T= | GRCh37 |
NC_000011.8:g.67560662T= | NCBI36 |
NG_007878.1:g.2604T= , LRG_115:g.2604T= | |
NG_017040.1:g.11003T= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000313468.10:c.*26T= MANE Select | ENSP00000315774.5:n.*26T= | |
ENST00000313468.9:c.*26T= | ENSP00000315774.5:n.*26T= | |
ENST00000524810.5:c.591T= | ||
ENST00000528492.1:c.*26T= | ENSP00000432848.1:n.*26T= | |
ENST00000531282.1:n.511T= | ||
NM_002496.3:c.*26T= | NP_002487.1:n.*26T= | |
XM_005274013.1:c.*26T= | XP_005274070.1:n.*26T= | |
XM_005274014.1:c.*26T= | XP_005274071.1:n.*26T= | |
XM_005274015.1:c.*26T= | XP_005274072.1:n.*26T= | |
XM_011545053.1:c.*26T= | XP_011543355.1:n.*26T= | |
NM_002496.4:c.*26T= MANE Select | NP_002487.1:n.*26T= |