HGVS | Genome Assembly |
---|---|
NC_000006.12:g.24145297T>C , CM000668.2:g.24145297T>C | GRCh38 |
NC_000006.11:g.24145525T>C , CM000668.1:g.24145525T>C | GRCh37 |
NC_000006.10:g.24253504T>C | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000378491.9:c.190-251T>C MANE Select | ENSP00000367752.4:n.190-251T>C | |
ENST00000378477.2:c.190-251T>C | ENSP00000367738.2:n.190-251T>C | |
ENST00000378478.5:c.190-251T>C | ENSP00000367739.2:n.190-251T>C | |
ENST00000378491.8:c.190-251T>C | ENSP00000367752.4:n.190-251T>C | |
ENST00000468195.2:n.257-9474T>C | ||
NM_080723.4:c.190-251T>C | NP_542454.3:n.190-251T>C | |
NM_080723.5:c.190-251T>C MANE Select | NP_542454.3:n.190-251T>C |