HGVS | Genome Assembly |
---|---|
NC_000016.10:g.30737286T= , CM000678.2:g.30737286T= | GRCh38 |
NC_000016.9:g.30748607T= , CM000678.1:g.30748607T= | GRCh37 |
NC_000016.8:g.30656108T= | NCBI36 |
NG_032135.1:g.43146T= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000411466.7:c.7246T= | ENSP00000405186.3:p.Ser2416= | |
ENST00000704023.1:c.1526T= | ||
ENST00000706321.1:c.7246T= | ENSP00000516346.1:p.Ser2416= | |
ENST00000262518.9:c.7246T= MANE Select | ENSP00000262518.4:p.Ser2416= | |
ENST00000262518.8:c.7246T= | ENSP00000262518.4:p.Ser2416= | |
ENST00000380361.7:c.6715T= | ENSP00000369719.3:p.Ser2239= | |
ENST00000395059.6:c.6469T= | ENSP00000378499.3:p.Ser2157= | |
NM_006662.2:c.7246T= | NP_006653.2:p.Ser2416= | |
NM_006662.3:c.7246T= MANE Select | NP_006653.2:p.Ser2416= |