HGVS | Genome Assembly |
---|---|
NC_000001.11:g.15445741A>G , CM000663.2:g.15445741A>G | GRCh38 |
NC_000001.10:g.15772236A>G , CM000663.1:g.15772236A>G | GRCh37 |
NC_000001.9:g.15644823A>G | NCBI36 |
NG_009253.1:g.12299A>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000375949.5:c.784A>G MANE Select | ENSP00000365116.4:p.Ile262Val | |
ENST00000375943.6:c.*238A>G | ENSP00000365110.2:n.*238A>G | |
ENST00000375949.4:c.784A>G | ENSP00000365116.4:p.Ile262Val | |
ENST00000483406.1:n.548A>G | ||
NM_007272.2:c.784A>G | NP_009203.2:p.Ile262Val | |
XM_011540550.1:c.638A>G | XP_011538852.1:p.Asp213Gly | |
NM_007272.3:c.784A>G MANE Select | NP_009203.2:p.Ile262Val |