HGVS | Genome Assembly |
---|---|
NC_000005.10:g.128395203T>G , CM000667.2:g.128395203T>G | GRCh38 |
NC_000005.9:g.127730896T>G , CM000667.1:g.127730896T>G | GRCh37 |
NC_000005.8:g.127758795T>G | NCBI36 |
NG_008750.1:g.147840A>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000703787.1:n.857A>C | ||
ENST00000262464.9:c.1150A>C MANE Select | ENSP00000262464.4:p.Thr384Pro | |
ENST00000262464.8:c.1150A>C | ENSP00000262464.4:p.Thr384Pro | |
ENST00000508053.5:c.1150A>C | ENSP00000424571.1:p.Thr384Pro | |
ENST00000508989.5:c.1051A>C | ENSP00000425596.1:p.Thr351Pro | |
ENST00000619499.4:c.1147A>C | ENSP00000482132.1:p.Thr383Pro | |
NM_001999.3:c.1150A>C | NP_001990.2:p.Thr384Pro | |
XM_017009228.2:c.1079-1835A>C | XP_016864717.1:n.1079-1835A>C | |
NM_001999.4:c.1150A>C MANE Select | NP_001990.2:p.Thr384Pro |