HGVS | Genome Assembly |
---|---|
NC_000019.10:g.40845267A= , CM000681.2:g.40845267A= | GRCh38 |
NC_000019.9:g.41351172A= , CM000681.1:g.41351172A= | GRCh37 |
NC_000019.8:g.46043012A= | NCBI36 |
NG_008377.1:g.10181T= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000301141.10:c.1161+27T= MANE Select | ENSP00000301141.4:n.1161+27T= | |
ENST00000301141.9:c.1161+27T= | ENSP00000301141.4:n.1161+27T= | |
ENST00000596719.5:n.1039T= | ||
ENST00000601627.1:c.119+43852A= | ||
ENST00000610301.1:c.1161+27T= | ENSP00000477899.1:n.1161+27T= | |
NM_000762.5:c.1161+27T= | NP_000753.3:n.1161+27T= | |
NM_000762.6:c.1161+27T= MANE Select | NP_000753.3:n.1161+27T= |