HGVS | Genome Assembly |
---|---|
NC_000008.11:g.19951814C= , CM000670.2:g.19951814C= | GRCh38 |
NC_000008.10:g.19809325C= , CM000670.1:g.19809325C= | GRCh37 |
NC_000008.9:g.19853605C= | NCBI36 |
NG_008855.1:g.17744C= | |
NG_008855.2:g.55098C= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000650287.1:c.295C= MANE Select | ENSP00000497642.1:p.Leu99= | |
ENST00000311322.8:c.295C= | ENSP00000309757.6:p.Leu99= | |
ENST00000520959.5:c.67C= | ENSP00000428496.1:p.Leu23= | |
ENST00000521994.1:n.552C= | ||
ENST00000522701.5:c.295C= | ENSP00000428557.1:p.Leu99= | |
ENST00000524029.5:c.295C= | ENSP00000428237.1:p.Leu99= | |
NM_000237.2:c.295C= | NP_000228.1:p.Leu99= | |
NM_000237.3:c.295C= MANE Select | NP_000228.1:p.Leu99= |