HGVS | Genome Assembly |
---|---|
NC_000023.11:g.25013741A>C , CM000685.2:g.25013741A>C | GRCh38 |
NC_000023.10:g.25031858A>C , CM000685.1:g.25031858A>C | GRCh37 |
NC_000023.9:g.24941779A>C | NCBI36 |
NG_008281.1:g.7208T>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000379044.5:c.254T>G MANE Select | ENSP00000368332.4:p.Leu85Arg | |
ENST00000379044.4:c.254T>G | ENSP00000368332.4:p.Leu85Arg | |
NM_139058.2:c.254T>G | NP_620689.1:p.Leu85Arg | |
NM_139058.3:c.254T>G MANE Select | NP_620689.1:p.Leu85Arg |