HGVS | Genome Assembly |
---|---|
NC_000019.10:g.40848629G= , CM000681.2:g.40848629G= | GRCh38 |
NC_000019.9:g.41354534G= , CM000681.1:g.41354534G= | GRCh37 |
NC_000019.8:g.46046374G= | NCBI36 |
NG_008377.1:g.6819C= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000301141.10:c.478C= MANE Select | ENSP00000301141.4:p.Leu160= | |
ENST00000301141.9:c.478C= | ENSP00000301141.4:p.Leu160= | |
ENST00000596719.5:n.329C= | ||
ENST00000600495.1:c.*290C= | ENSP00000472905.1:n.*290C= | |
ENST00000601627.1:c.120-43362G= | ||
ENST00000610301.1:c.478C= | ENSP00000477899.1:p.Leu160= | |
NM_000762.5:c.478C= | NP_000753.3:p.Leu160= | |
NM_000762.6:c.478C= MANE Select | NP_000753.3:p.Leu160= |