HGVS | Genome Assembly |
---|---|
NC_000005.10:g.128261861G= , CM000667.2:g.128261861G= | GRCh38 |
NC_000005.9:g.127597553G= , CM000667.1:g.127597553G= | GRCh37 |
NC_000005.8:g.127625452G= | NCBI36 |
NG_008750.1:g.281183C= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000262464.9:c.8239C= MANE Select | ENSP00000262464.4:p.Leu2747= | |
ENST00000262464.8:c.8239C= | ENSP00000262464.4:p.Leu2747= | |
ENST00000508053.5:c.8239C= | ENSP00000424571.1:p.Leu2747= | |
ENST00000619499.4:c.8236C= | ENSP00000482132.1:p.Leu2746= | |
NM_001999.3:c.8239C= | NP_001990.2:p.Leu2747= | |
XM_017009228.2:c.8086C= | XP_016864717.1:p.Leu2696= | |
NM_001999.4:c.8239C= MANE Select | NP_001990.2:p.Leu2747= |