HGVS | Genome Assembly |
---|---|
NC_000021.9:g.43172011T= , CM000683.2:g.43172011T= | GRCh38 |
NG_009823.1:g.7981T= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000291554.6:c.313-60T= MANE Select | ENSP00000291554.2:n.313-60T= | |
ENST00000398132.1:c.202-60T= | ENSP00000381200.1:n.202-60T= | |
ENST00000398133.5:c.253-60T= | ENSP00000381201.1:n.253-60T= | |
ENST00000468016.1:n.414-60T= | ||
ENST00000482775.1:n.394-60T= | ||
NM_000394.3:c.313-60T= | NP_000385.1:n.313-60T= | |
XM_005261093.2:c.202-60T= | XP_005261150.1:n.202-60T= | |
NM_001363766.1:c.202-60T= | NP_001350695.1:n.202-60T= | |
NM_000394.4:c.313-60T= MANE Select | NP_000385.1:n.313-60T= |