HGVS | Genome Assembly |
---|---|
NC_000010.11:g.97611592T>A , CM000672.2:g.97611592T>A | GRCh38 |
NC_000010.10:g.99371349T>A , CM000672.1:g.99371349T>A | GRCh37 |
NC_000010.9:g.99361339T>A | NCBI36 |
NG_027922.1:g.32248T>A |
HGVS | Amino-acid change | |
---|---|---|
ENST00000370646.9:c.917T>A MANE Select | ENSP00000359680.4:p.Leu306Ter | |
ENST00000370646.8:c.917T>A | ENSP00000359680.4:p.Leu306Ter | |
ENST00000370647.8:c.428T>A | ENSP00000359681.4:p.Leu143Ter | |
ENST00000370649.3:c.345+9602T>A | ENSP00000359683.3:n.345+9602T>A | |
NM_001134670.1:c.428T>A | NP_001128142.1:p.Leu143Ter | |
NM_138413.3:c.917T>A | NP_612422.2:p.Leu306Ter | |
NM_138413.4:c.917T>A MANE Select | NP_612422.2:p.Leu306Ter | |
NM_001134670.2:c.428T>A | NP_001128142.1:p.Leu143Ter |