HGVS | Genome Assembly |
---|---|
NC_000005.10:g.6611068C= , CM000667.2:g.6611068C= | GRCh38 |
NC_000005.9:g.6611181C= , CM000667.1:g.6611181C= | GRCh37 |
NC_000005.8:g.6664181C= | NCBI36 |
NG_028215.1:g.27293G= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000264670.11:c.1113G= MANE Select | ENSP00000264670.6:p.Gly371= | |
ENST00000264670.10:c.1113G= | ENSP00000264670.6:p.Gly371= | |
ENST00000504374.5:c.*419G= | ENSP00000421783.1:n.*419G= | |
ENST00000505892.5:n.1682G= | ||
ENST00000506139.5:c.1008G= | ENSP00000420957.1:p.Gly336= | |
NM_001193455.1:c.1008G= | NP_001180384.1:p.Gly336= | |
NM_017755.5:c.1113G= | NP_060225.4:p.Gly371= | |
NR_037947.1:n.1409G= | ||
NM_017755.6:c.1113G= MANE Select | NP_060225.4:p.Gly371= | |
NM_001193455.2:c.1008G= | NP_001180384.1:p.Gly336= | |
NR_037947.2:n.1093G= |