HGVS | Genome Assembly |
---|---|
NC_000002.12:g.202514973G= , CM000664.2:g.202514973G= | GRCh38 |
NC_000002.11:g.203379696G= , CM000664.1:g.203379696G= | GRCh37 |
NC_000002.10:g.203087941G= | NCBI36 |
NG_009363.1:g.143647G= , LRG_712:g.143647G= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000374580.10:c.615G= MANE Select | ENSP00000363708.4:p.Leu205= | |
ENST00000638587.1:c.546G= | ENSP00000491062.1:p.Leu182= | |
ENST00000374574.2:c.615G= | ENSP00000363702.2:p.Leu205= | |
ENST00000374580.8:c.615G= | ENSP00000363708.4:p.Leu205= | |
NM_001204.6:c.615G= , LRG_712t1:c.615G= | NP_001195.2:p.Leu205= | |
XM_011511687.1:c.615G= | XP_011509989.1:p.Leu205= | |
XM_011511688.1:c.615G= | XP_011509990.1:p.Leu205= | |
NM_001204.7:c.615G= MANE Select | NP_001195.2:p.Leu205= |