HGVS | Genome Assembly |
---|---|
NC_000015.10:g.64160111G= , CM000677.2:g.64160111G= | GRCh38 |
NC_000015.9:g.64452310G= , CM000677.1:g.64452310G= | GRCh37 |
NC_000015.8:g.62239363G= | NCBI36 |
NG_012979.1:g.8045C= , LRG_10:g.8045C= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000300026.4:c.336C= MANE Select | ENSP00000300026.4:p.Gly112= | |
ENST00000561048.2:n.369C= | ||
ENST00000680158.1:c.336C= | ENSP00000504873.1:p.Gly112= | |
ENST00000680343.1:n.290C= | ||
ENST00000681397.1:c.336C= | ENSP00000506584.1:p.Gly112= | |
ENST00000681658.1:c.231C= | ENSP00000505431.1:p.Gly77= | |
ENST00000300026.3:c.336C= | ENSP00000300026.3:p.Gly112= | |
ENST00000558492.1:n.242C= | ||
ENST00000561048.1:n.371C= | ||
NM_000942.4:c.336C= , LRG_10t1:c.336C= | NP_000933.1:p.Gly112= | |
NM_000942.5:c.336C= MANE Select | NP_000933.1:p.Gly112= |