HGVS | Genome Assembly |
---|---|
NC_000015.10:g.43068030T>C , CM000677.2:g.43068030T>C | GRCh38 |
NC_000015.9:g.43360228T>C , CM000677.1:g.43360228T>C | GRCh37 |
NC_000015.8:g.41147520T>C | NCBI36 |
NG_012182.1:g.43059A>G |
HGVS | Amino-acid change | |
---|---|---|
ENST00000290650.9:c.666A>G MANE Select | ENSP00000290650.4:p.Lys222= | |
ENST00000290650.8:c.666A>G | ENSP00000290650.4:p.Lys222= | |
ENST00000546274.6:c.666A>G | ENSP00000477932.1:p.Lys222= | |
ENST00000563239.1:c.*202+2869A>G | ENSP00000456502.1:n.*202+2869A>G | |
NM_174916.2:c.666A>G | NP_777576.1:p.Lys222= | |
NM_174916.3:c.666A>G MANE Select | NP_777576.1:p.Lys222= |