HGVS | Genome Assembly |
---|---|
NC_000012.12:g.91055900G>A , CM000674.2:g.91055900G>A | GRCh38 |
NC_000012.11:g.91449677G>A , CM000674.1:g.91449677G>A | GRCh37 |
NC_000012.10:g.89973808G>A | NCBI36 |
NG_021223.1:g.7455C>T , LRG_538:g.7455C>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000266719.4:c.382C>T MANE Select | ENSP00000266719.3:p.Leu128= | |
ENST00000266719.3:c.382C>T | ENSP00000266719.3:p.Leu128= | |
NM_007035.3:c.382C>T , LRG_538t1:c.382C>T | NP_008966.1:p.Leu128= | |
XM_011537781.1:c.382C>T | XP_011536083.1:p.Leu128= | |
NM_007035.4:c.382C>T MANE Select | NP_008966.1:p.Leu128= |