HGVS | Genome Assembly |
---|---|
NC_000012.12:g.4912657T= , CM000674.2:g.4912657T= | GRCh38 |
NC_000012.11:g.5021823T= , CM000674.1:g.5021823T= | GRCh37 |
NC_000012.10:g.4892084T= | NCBI36 |
NG_011815.1:g.7751T= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000382545.5:c.1279T= MANE Select | ENSP00000371985.3:p.Leu427= | |
ENST00000543874.3:n.105+2185T= | ||
ENST00000639306.1:c.1117T= | ENSP00000492506.1:p.Leu373= | |
ENST00000639680.1:c.76+391T= | ||
ENST00000382545.3:c.1279T= | ENSP00000371985.3:p.Leu427= | |
ENST00000541095.1:n.105+2185T= | ||
ENST00000543874.2:n.96+2185T= | ||
NM_000217.2:c.1279T= | NP_000208.2:p.Leu427= | |
NM_000217.3:c.1279T= MANE Select | NP_000208.2:p.Leu427= |