HGVS | Genome Assembly |
---|---|
NC_000006.12:g.111222840A>G , CM000668.2:g.111222840A>G | GRCh38 |
NC_000006.11:g.111544043A>G , CM000668.1:g.111544043A>G | GRCh37 |
NC_000006.10:g.111650736A>G | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000368851.10:c.*605A>G MANE Select | ENSP00000357844.4:n.*605A>G | |
ENST00000368850.4:c.*605A>G | ENSP00000357843.1:n.*605A>G | |
ENST00000368851.9:c.*605A>G | ENSP00000357844.4:n.*605A>G | |
NM_018593.4:c.*605A>G | NP_061063.2:n.*605A>G | |
XM_005266818.2:c.*559A>G | XP_005266875.1:n.*559A>G | |
XM_017010237.1:c.*605A>G | XP_016865726.1:n.*605A>G | |
XR_001743158.1:n.2435A>G | ||
NM_018593.5:c.*605A>G MANE Select | NP_061063.2:n.*605A>G |