HGVS | Genome Assembly |
---|---|
NC_000005.10:g.128261596T= , CM000667.2:g.128261596T= | GRCh38 |
NC_000005.9:g.127597288T= , CM000667.1:g.127597288T= | GRCh37 |
NC_000005.8:g.127625187T= | NCBI36 |
NG_008750.1:g.281448A= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000262464.9:c.8364+140A= MANE Select | ENSP00000262464.4:n.8364+140A= | |
ENST00000262464.8:c.8364+140A= | ENSP00000262464.4:n.8364+140A= | |
ENST00000508053.5:c.8364+140A= | ENSP00000424571.1:n.8364+140A= | |
ENST00000619499.4:c.8361+140A= | ENSP00000482132.1:n.8361+140A= | |
NM_001999.3:c.8364+140A= | NP_001990.2:n.8364+140A= | |
XM_017009228.2:c.8211+140A= | XP_016864717.1:n.8211+140A= | |
NM_001999.4:c.8364+140A= MANE Select | NP_001990.2:n.8364+140A= |