HGVS | Genome Assembly |
---|---|
NC_000019.10:g.40848254C>A , CM000681.2:g.40848254C>A | GRCh38 |
NC_000019.9:g.41354159C>A , CM000681.1:g.41354159C>A | GRCh37 |
NC_000019.8:g.46045999C>A | NCBI36 |
NG_008377.1:g.7194G>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000301141.10:c.619G>T MANE Select | ENSP00000301141.4:p.Gly207Ter | |
ENST00000301141.9:c.619G>T | ENSP00000301141.4:p.Gly207Ter | |
ENST00000596719.5:n.470G>T | ||
ENST00000600495.1:c.*431G>T | ENSP00000472905.1:n.*431G>T | |
ENST00000601627.1:c.120-43737C>A | ||
ENST00000610301.1:c.619G>T | ENSP00000477899.1:p.Gly207Ter | |
NM_000762.5:c.619G>T | NP_000753.3:p.Gly207Ter | |
NM_000762.6:c.619G>T MANE Select | NP_000753.3:p.Gly207Ter |