HGVS | Genome Assembly |
---|---|
NC_000006.12:g.33669093G>C , CM000668.2:g.33669093G>C | GRCh38 |
NC_000006.11:g.33636870G>C , CM000668.1:g.33636870G>C | GRCh37 |
NC_000006.10:g.33744848G>C | NCBI36 |
NG_027729.1:g.52715G>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000605930.3:c.2126G>C MANE Select | ENSP00000475177.1:p.Arg709Thr | |
ENST00000374316.9:c.2126G>C | ENSP00000363435.4:p.Arg709Thr | |
ENST00000605930.2:c.2126G>C | ENSP00000475177.1:p.Arg709Thr | |
NM_002224.3:c.2126G>C | NP_002215.2:p.Arg709Thr | |
XM_011514576.1:c.2195G>C | XP_011512878.1:p.Arg732Thr | |
XM_011514577.1:c.1943G>C | XP_011512879.1:p.Arg648Thr | |
XM_011514577.3:c.1943G>C | XP_011512879.1:p.Arg648Thr | |
XM_017010832.1:c.2126G>C | XP_016866321.1:p.Arg709Thr | |
NM_002224.4:c.2126G>C MANE Select | NP_002215.2:p.Arg709Thr |