HGVS | Genome Assembly |
---|---|
NC_000008.11:g.96160291T= , CM000670.2:g.96160291T= | GRCh38 |
NC_000008.10:g.97172519T= , CM000670.1:g.97172519T= | GRCh37 |
NC_000008.9:g.97241695T= | NCBI36 |
NG_008981.1:g.5502A= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000287020.7:c.402A= MANE Select | ENSP00000287020.4:p.Gly134= | |
ENST00000287020.6:c.402A= | ENSP00000287020.4:p.Gly134= | |
ENST00000620978.1:c.402A= | ENSP00000480170.1:p.Gly134= | |
ENST00000621429.1:c.402A= | ENSP00000483711.1:p.Gly134= | |
NM_001001557.2:c.402A= | NP_001001557.1:p.Gly134= | |
NM_001001557.3:c.402A= | NP_001001557.1:p.Gly134= | |
NM_001001557.4:c.402A= MANE Select | NP_001001557.1:p.Gly134= |