HGVS | Genome Assembly |
---|---|
NC_000005.10:g.128357391T>C , CM000667.2:g.128357391T>C | GRCh38 |
NC_000005.9:g.127693083T>C , CM000667.1:g.127693083T>C | GRCh37 |
NC_000005.8:g.127720982T>C | NCBI36 |
NG_008750.1:g.185653A>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000262464.9:c.2559A>G MANE Select | ENSP00000262464.4:p.Ile853Met | |
ENST00000262464.8:c.2559A>G | ENSP00000262464.4:p.Ile853Met | |
ENST00000508053.5:c.2559A>G | ENSP00000424571.1:p.Ile853Met | |
ENST00000508989.5:c.2460A>G | ENSP00000425596.1:p.Ile820Met | |
ENST00000619499.4:c.2556A>G | ENSP00000482132.1:p.Ile852Met | |
NM_001999.3:c.2559A>G | NP_001990.2:p.Ile853Met | |
XM_017009228.2:c.2406A>G | XP_016864717.1:p.Ile802Met | |
NM_001999.4:c.2559A>G MANE Select | NP_001990.2:p.Ile853Met |