HGVS | Genome Assembly |
---|---|
NC_000023.11:g.154837621G>C , CM000685.2:g.154837621G>C | GRCh38 |
NC_000023.10:g.154065896G>C , CM000685.1:g.154065896G>C | GRCh37 |
NC_000023.9:g.153719090G>C | NCBI36 |
NG_011403.1:g.190103C>G | |
NG_033065.1:g.2042C>G | |
NG_011403.2:g.190103C>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000360256.9:c.7032C>G MANE Select | ENSP00000353393.4:p.Gly2344= | |
ENST00000644698.1:c.765C>G | ENSP00000495706.1:p.Gly255= | |
ENST00000330287.10:c.627C>G | ENSP00000327895.6:p.Gly209= | |
ENST00000360256.8:c.7032C>G | ENSP00000353393.4:p.Gly2344= | |
NM_000132.3:c.7032C>G | NP_000123.1:p.Gly2344= | |
NM_019863.2:c.627C>G | NP_063916.1:p.Gly209= | |
XM_011531126.1:c.6927C>G | XP_011529428.1:p.Gly2309= | |
NM_000132.4:c.7032C>G MANE Select | NP_000123.1:p.Gly2344= | |
NM_019863.3:c.627C>G | NP_063916.1:p.Gly209= |