HGVS | Genome Assembly |
---|---|
NC_000005.10:g.128357310G>A , CM000667.2:g.128357310G>A | GRCh38 |
NC_000005.9:g.127693002G>A , CM000667.1:g.127693002G>A | GRCh37 |
NC_000005.8:g.127720901G>A | NCBI36 |
NG_008750.1:g.185734C>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000262464.9:c.2640C>T MANE Select | ENSP00000262464.4:p.Gly880= | |
ENST00000262464.8:c.2640C>T | ENSP00000262464.4:p.Gly880= | |
ENST00000508053.5:c.2640C>T | ENSP00000424571.1:p.Gly880= | |
ENST00000508989.5:c.2541C>T | ENSP00000425596.1:p.Gly847= | |
ENST00000619499.4:c.2637C>T | ENSP00000482132.1:p.Gly879= | |
NM_001999.3:c.2640C>T | NP_001990.2:p.Gly880= | |
XM_017009228.2:c.2487C>T | XP_016864717.1:p.Gly829= | |
NM_001999.4:c.2640C>T MANE Select | NP_001990.2:p.Gly880= |