HGVS | Genome Assembly |
---|---|
NC_000005.10:g.128300897G>A , CM000667.2:g.128300897G>A | GRCh38 |
NC_000005.9:g.127636589G>A , CM000667.1:g.127636589G>A | GRCh37 |
NC_000005.8:g.127664488G>A | NCBI36 |
NG_008750.1:g.242147C>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000703783.1:n.2870C>T | ||
ENST00000703785.1:n.2789C>T | ||
ENST00000262464.9:c.6086C>T MANE Select | ENSP00000262464.4:p.Pro2029Leu | |
ENST00000262464.8:c.6086C>T | ENSP00000262464.4:p.Pro2029Leu | |
ENST00000508053.5:c.6086C>T | ENSP00000424571.1:p.Pro2029Leu | |
ENST00000619499.4:c.6083C>T | ENSP00000482132.1:p.Pro2028Leu | |
NM_001999.3:c.6086C>T | NP_001990.2:p.Pro2029Leu | |
XM_017009228.2:c.5933C>T | XP_016864717.1:p.Pro1978Leu | |
NM_001999.4:c.6086C>T MANE Select | NP_001990.2:p.Pro2029Leu |