HGVS | Genome Assembly |
---|---|
NC_000011.10:g.47582460T>A , CM000673.2:g.47582460T>A | GRCh38 |
NC_000011.9:g.47604012T>A , CM000673.1:g.47604012T>A | GRCh37 |
NC_000011.8:g.47560588T>A | NCBI36 |
NG_011946.1:g.8451T>A | |
NG_011946.2:g.8451T>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000263774.9:c.619T>A MANE Select | ENSP00000263774.4:p.Tyr207Asn | |
ENST00000531351.2:n.1814T>A | ||
ENST00000677462.1:n.3093T>A | ||
ENST00000678975.1:n.2876T>A | ||
ENST00000263774.8:c.619T>A | ENSP00000263774.4:p.Tyr207Asn | |
ENST00000524568.1:n.722T>A | ||
ENST00000525212.1:n.274T>A | ||
ENST00000525378.5:n.557T>A | ||
ENST00000527178.1:n.219T>A | ||
ENST00000533507.5:n.1513T>A | ||
NM_004551.2:c.619T>A | NP_004542.1:p.Tyr207Asn | |
NM_004551.3:c.619T>A MANE Select | NP_004542.1:p.Tyr207Asn |