HGVS | Genome Assembly |
---|---|
NC_000010.11:g.43130265A= , CM000672.2:g.43130265A= | GRCh38 |
NC_000010.10:g.43625713A= , CM000672.1:g.43625713A= | GRCh37 |
NC_000010.9:g.42945719A= | NCBI36 |
NG_007489.1:g.58197A= , LRG_518:g.58197A= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000615310.5:c.*3511A= | ENSP00000480088.2:n.*3511A= | |
ENST00000683007.1:n.6304A= | ||
ENST00000355710.8:c.*1996A= MANE Select | ENSP00000347942.3:n.*1996A= | |
ENST00000355710.7:c.*1996A= | ENSP00000347942.3:n.*1996A= | |
ENST00000615310.4:c.*2690A= | ENSP00000480088.1:n.*2690A= | |
NM_020975.4:c.*1996A= , LRG_518t1:c.*1996A= | NP_066124.1:n.*1996A= | |
XM_011540027.1:c.*764A= | XP_011538329.1:n.*764A= | |
NM_020975.5:c.*1996A= | NP_066124.1:n.*1996A= | |
NM_020975.6:c.*1996A= MANE Select | NP_066124.1:n.*1996A= |