HGVS | Genome Assembly |
---|---|
NC_000012.12:g.102852826A= , CM000674.2:g.102852826A= | GRCh38 |
NC_000012.11:g.103246604A= , CM000674.1:g.103246604A= | GRCh37 |
NC_000012.10:g.101770734A= | NCBI36 |
NG_008690.1:g.69777T= | |
NG_008690.2:g.110585T= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000553106.6:c.831T= MANE Select | ENSP00000448059.1:p.Tyr277= | |
ENST00000307000.7:c.816T= | ENSP00000303500.2:p.Tyr272= | |
ENST00000549247.6:n.590T= | ||
ENST00000553106.5:c.831T= | ENSP00000448059.1:p.Tyr277= | |
NM_000277.1:c.831T= | NP_000268.1:p.Tyr277= | |
XM_011538422.1:c.831T= | XP_011536724.1:p.Tyr277= | |
NM_000277.2:c.831T= | NP_000268.1:p.Tyr277= | |
NM_001354304.1:c.831T= | NP_001341233.1:p.Tyr277= | |
NM_000277.3:c.831T= MANE Select | NP_000268.1:p.Tyr277= | |
NM_001354304.2:c.831T= | NP_001341233.1:p.Tyr277= |