HGVS | Genome Assembly |
---|---|
NC_000002.12:g.96293089A>C , CM000664.2:g.96293089A>C | GRCh38 |
NC_000002.11:g.96958827A>C , CM000664.1:g.96958827A>C | GRCh37 |
NC_000002.10:g.96322554A>C | NCBI36 |
NG_016973.1:g.17471T>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000323853.10:c.2043T>G MANE Select | ENSP00000317123.5:p.Arg681= | |
ENST00000652267.1:c.2043T>G | ENSP00000498933.1:p.Arg681= | |
ENST00000323853.9:c.2043T>G | ENSP00000317123.5:p.Arg681= | |
NM_014014.4:c.2043T>G | NP_054733.2:p.Arg681= | |
NM_014014.5:c.2043T>G MANE Select | NP_054733.2:p.Arg681= |