HGVS | Genome Assembly |
---|---|
NC_000015.10:g.38356503G>T , CM000677.2:g.38356503G>T | GRCh38 |
NC_000015.9:g.38648704G>T , CM000677.1:g.38648704G>T | GRCh37 |
NC_000015.8:g.36435996G>T | NCBI36 |
NG_008980.1:g.108653G>T |
HGVS | Amino-acid change | |
---|---|---|
ENST00000299084.9:c.*4839G>T MANE Select | ENSP00000299084.4:n.*4839G>T | |
ENST00000299084.8:c.*4839G>T | ENSP00000299084.4:n.*4839G>T | |
NM_152594.2:c.*4839G>T | NP_689807.1:n.*4839G>T | |
XM_005254202.3:c.*4839G>T | XP_005254259.1:n.*4839G>T | |
XM_011521289.3:c.*4839G>T | XP_011519591.1:n.*4839G>T | |
NM_152594.3:c.*4839G>T MANE Select | NP_689807.1:n.*4839G>T |