HGVS | Genome Assembly |
---|---|
NC_000023.11:g.83508928A>C , CM000685.2:g.83508928A>C | GRCh38 |
NC_000023.10:g.82763936A>C , CM000685.1:g.82763936A>C | GRCh37 |
NC_000023.9:g.82650592A>C | NCBI36 |
NG_009936.2:g.5668A>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000644024.2:c.604A>C MANE Select | ENSP00000495996.1:p.Lys202Gln | |
ENST00000373200.4:c.604A>C | ENSP00000362296.2:p.Lys202Gln | |
NM_000307.4:c.604A>C | NP_000298.3:p.Lys202Gln | |
NM_000307.5:c.604A>C MANE Select | NP_000298.3:p.Lys202Gln |