HGVS | Genome Assembly |
---|---|
NC_000012.12:g.91055847T= , CM000674.2:g.91055847T= | GRCh38 |
NC_000012.11:g.91449624T= , CM000674.1:g.91449624T= | GRCh37 |
NC_000012.10:g.89973755T= | NCBI36 |
NG_021223.1:g.7508A= , LRG_538:g.7508A= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000266719.4:c.435A= MANE Select | ENSP00000266719.3:p.Glu145= | |
ENST00000266719.3:c.435A= | ENSP00000266719.3:p.Glu145= | |
NM_007035.3:c.435A= , LRG_538t1:c.435A= | NP_008966.1:p.Glu145= | |
XM_011537781.1:c.435A= | XP_011536083.1:p.Glu145= | |
NM_007035.4:c.435A= MANE Select | NP_008966.1:p.Glu145= |