HGVS | Genome Assembly |
---|---|
NC_000015.10:g.64160107C= , CM000677.2:g.64160107C= | GRCh38 |
NC_000015.9:g.64452306C= , CM000677.1:g.64452306C= | GRCh37 |
NC_000015.8:g.62239359C= | NCBI36 |
NG_012979.1:g.8049G= , LRG_10:g.8049G= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000300026.4:c.340G= MANE Select | ENSP00000300026.4:p.Gly114= | |
ENST00000561048.2:n.373G= | ||
ENST00000680158.1:c.340G= | ENSP00000504873.1:p.Gly114= | |
ENST00000680343.1:n.294G= | ||
ENST00000681397.1:c.340G= | ENSP00000506584.1:p.Gly114= | |
ENST00000681658.1:c.235G= | ENSP00000505431.1:p.Gly79= | |
ENST00000300026.3:c.340G= | ENSP00000300026.3:p.Gly114= | |
ENST00000558492.1:n.246G= | ||
ENST00000561048.1:n.375G= | ||
NM_000942.4:c.340G= , LRG_10t1:c.340G= | NP_000933.1:p.Gly114= | |
NM_000942.5:c.340G= MANE Select | NP_000933.1:p.Gly114= |