HGVS | Genome Assembly |
---|---|
NC_000005.10:g.111119018T>C , CM000667.2:g.111119018T>C | GRCh38 |
NC_000005.9:g.110454716T>C , CM000667.1:g.110454716T>C | GRCh37 |
NC_000005.8:g.110482615T>C | NCBI36 |
NG_008979.1:g.31847T>C |
HGVS | Amino-acid change | |
---|---|---|
ENST00000513710.4:c.1802T>C MANE Select | ENSP00000424628.3:p.Ile601Thr | |
ENST00000506538.6:c.1970T>C | ENSP00000423067.2:p.Ile657Thr | |
ENST00000513710.3:c.1802T>C | ENSP00000424628.3:p.Ile601Thr | |
ENST00000612402.4:c.1970T>C | ENSP00000479950.1:p.Ile657Thr | |
NM_139281.2:c.1970T>C | NP_644810.1:p.Ile657Thr | |
XM_011543163.1:c.1970T>C | XP_011541465.1:p.Ile657Thr | |
NM_139281.3:c.1802T>C MANE Select | NP_644810.2:p.Ile601Thr |