HGVS | Genome Assembly |
---|---|
NC_000001.11:g.197039162A= , CM000663.2:g.197039162A= | GRCh38 |
NC_000001.10:g.197008292A= , CM000663.1:g.197008292A= | GRCh37 |
NC_000001.9:g.195274915A= | NCBI36 |
NG_012065.1:g.33106T= , LRG_550:g.33106T= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000367412.2:c.*216T= MANE Select | ENSP00000356382.2:n.*216T= | |
ENST00000649282.1:c.957T= | ENSP00000497116.1:n.957T= | |
XM_011509283.2:c.*1137T= | XP_011507585.1:n.*1137T= | |
XM_011509284.2:c.*1137T= | XP_011507586.1:n.*1137T= | |
XM_011509286.2:c.*1137T= | XP_011507588.1:n.*1137T= | |
NM_001994.3:c.*216T= MANE Select | NP_001985.2:n.*216T= |