HGVS | Genome Assembly |
---|---|
NC_000002.12:g.26519093G= , CM000664.2:g.26519093G= | GRCh38 |
NC_000002.11:g.26741961G= , CM000664.1:g.26741961G= | GRCh37 |
NC_000002.10:g.26595465G= | NCBI36 |
NG_009937.1:g.44606C= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000272371.7:c.244C= MANE Select | ENSP00000272371.2:p.Arg82= | |
ENST00000272371.6:c.244C= | ENSP00000272371.2:p.Arg82= | |
ENST00000403946.7:c.244C= | ENSP00000385255.3:p.Arg82= | |
NM_001287489.1:c.244C= | NP_001274418.1:p.Arg82= | |
NM_194248.2:c.244C= | NP_919224.1:p.Arg82= | |
XM_005264644.2:c.244C= | XP_005264701.1:p.Arg82= | |
XM_011533185.1:c.244C= | XP_011531487.1:p.Arg82= | |
XM_017005338.1:c.244C= | XP_016860827.1:p.Arg82= | |
NM_001287489.2:c.244C= | NP_001274418.1:p.Arg82= | |
NM_194248.3:c.244C= MANE Select | NP_919224.1:p.Arg82= |