HGVS | Genome Assembly |
---|---|
NC_000007.14:g.21816552T= , CM000669.2:g.21816552T= | GRCh38 |
NC_000007.13:g.21856170T= , CM000669.1:g.21856170T= | GRCh37 |
NC_000007.12:g.21822695T= | NCBI36 |
NG_012886.2:g.278338T= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000409508.8:c.10418T= MANE Select | ENSP00000475939.1:p.Leu3473= | |
ENST00000328843.10:c.10439T= | ENSP00000330671.7:p.Leu3480= | |
ENST00000409508.7:c.10418T= | ENSP00000475939.1:p.Leu3473= | |
ENST00000620169.4:c.10439T= | ENSP00000481693.1:p.Leu3480= | |
NM_001277115.1:c.10418T= | NP_001264044.1:p.Leu3473= | |
NM_001277115.2:c.10418T= MANE Select | NP_001264044.1:p.Leu3473= |