HGVS | Genome Assembly |
---|---|
NC_000012.12:g.52451645A= , CM000674.2:g.52451645A= | GRCh38 |
NC_000012.11:g.52845429A= , CM000674.1:g.52845429A= | GRCh37 |
NC_000012.10:g.51131696A= | NCBI36 |
NG_008299.1:g.5482T= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000252252.4:c.434T= MANE Select | ENSP00000252252.3:p.Leu145= | |
ENST00000252252.3:c.434T= | ENSP00000252252.3:p.Leu145= | |
NM_005555.3:c.434T= | NP_005546.2:p.Leu145= | |
NM_005555.4:c.434T= MANE Select | NP_005546.2:p.Leu145= |