HGVS | Genome Assembly |
---|---|
NC_000005.10:g.128300835T= , CM000667.2:g.128300835T= | GRCh38 |
NC_000005.9:g.127636527T= , CM000667.1:g.127636527T= | GRCh37 |
NC_000005.8:g.127664426T= | NCBI36 |
NG_008750.1:g.242209A= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000703783.1:n.2932A= | ||
ENST00000703785.1:n.2851A= | ||
ENST00000262464.9:c.6148A= MANE Select | ENSP00000262464.4:p.Lys2050= | |
ENST00000262464.8:c.6148A= | ENSP00000262464.4:p.Lys2050= | |
ENST00000508053.5:c.6148A= | ENSP00000424571.1:p.Lys2050= | |
ENST00000619499.4:c.6145A= | ENSP00000482132.1:p.Lys2049= | |
NM_001999.3:c.6148A= | NP_001990.2:p.Lys2050= | |
XM_017009228.2:c.5995A= | XP_016864717.1:p.Lys1999= | |
NM_001999.4:c.6148A= MANE Select | NP_001990.2:p.Lys2050= |