HGVS | Genome Assembly |
---|---|
NC_000023.11:g.64192858A>T , CM000685.2:g.64192858A>T | GRCh38 |
NC_000023.10:g.63412738A>T , CM000685.1:g.63412738A>T | GRCh37 |
NC_000023.9:g.63329463A>T | NCBI36 |
NG_021345.1:g.17887T>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000374869.8:c.429T>A MANE Select | ENSP00000364003.4:p.Cys143Ter | |
ENST00000330258.3:c.429T>A | ENSP00000329117.3:p.Cys143Ter | |
ENST00000374869.7:c.429T>A | ENSP00000364003.3:p.Cys143Ter | |
NM_152424.3:c.429T>A | NP_689637.3:p.Cys143Ter | |
XM_011530858.1:c.429T>A | XP_011529160.1:p.Cys143Ter | |
NM_152424.4:c.429T>A MANE Select | NP_689637.3:p.Cys143Ter |