HGVS | Genome Assembly |
---|---|
NC_000010.11:g.97611283G= , CM000672.2:g.97611283G= | GRCh38 |
NC_000010.10:g.99371040G= , CM000672.1:g.99371040G= | GRCh37 |
NC_000010.9:g.99361030G= | NCBI36 |
NG_027922.1:g.31939G= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000370646.9:c.835-227G= MANE Select | ENSP00000359680.4:n.835-227G= | |
ENST00000370646.8:c.835-227G= | ENSP00000359680.4:n.835-227G= | |
ENST00000370647.8:c.346-227G= | ENSP00000359681.4:n.346-227G= | |
ENST00000370649.3:c.345+9293G= | ENSP00000359683.3:n.345+9293G= | |
NM_001134670.1:c.346-227G= | NP_001128142.1:n.346-227G= | |
NM_138413.3:c.835-227G= | NP_612422.2:n.835-227G= | |
NM_138413.4:c.835-227G= MANE Select | NP_612422.2:n.835-227G= | |
NM_001134670.2:c.346-227G= | NP_001128142.1:n.346-227G= |