HGVS | Genome Assembly |
---|---|
NC_000015.10:g.43067926T>C , CM000677.2:g.43067926T>C | GRCh38 |
NC_000015.9:g.43360124T>C , CM000677.1:g.43360124T>C | GRCh37 |
NC_000015.8:g.41147416T>C | NCBI36 |
NG_012182.1:g.43163A>G |
HGVS | Amino-acid change | |
---|---|---|
ENST00000290650.9:c.770A>G MANE Select | ENSP00000290650.4:p.Gln257Arg | |
ENST00000290650.8:c.770A>G | ENSP00000290650.4:p.Gln257Arg | |
ENST00000546274.6:c.770A>G | ENSP00000477932.1:p.Gln257Arg | |
ENST00000563239.1:c.*202+2973A>G | ENSP00000456502.1:n.*202+2973A>G | |
NM_174916.2:c.770A>G | NP_777576.1:p.Gln257Arg | |
NM_174916.3:c.770A>G MANE Select | NP_777576.1:p.Gln257Arg |