HGVS | Genome Assembly |
---|---|
NC_000002.12:g.189008927T= , CM000664.2:g.189008927T= | GRCh38 |
NC_000002.11:g.189873653T= , CM000664.1:g.189873653T= | GRCh37 |
NC_000002.10:g.189581898T= | NCBI36 |
NG_007404.1:g.39555T= , LRG_3:g.39555T= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000450867.2:c.3430T= | ENSP00000415346.2:p.Ser1144= | |
ENST00000304636.9:c.3529T= MANE Select | ENSP00000304408.4:p.Ser1177= | |
ENST00000304636.7:c.3529T= | ENSP00000304408.3:p.Ser1177= | |
ENST00000317840.9:c.2620T= | ENSP00000315243.6:p.Ser874= | |
ENST00000487010.1:n.626T= | ||
NM_000090.3:c.3529T= , LRG_3t1:c.3529T= | NP_000081.1:p.Ser1177= | |
NM_000090.4:c.3529T= MANE Select | NP_000081.2:p.Ser1177= |