HGVS | Genome Assembly |
---|---|
NC_000015.10:g.43048389T>C , CM000677.2:g.43048389T>C | GRCh38 |
NC_000015.9:g.43340587T>C , CM000677.1:g.43340587T>C | GRCh37 |
NC_000015.8:g.41127879T>C | NCBI36 |
NG_012182.1:g.62700A>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000290650.9:c.1539+3A>G MANE Select | ENSP00000290650.4:n.1539+3A>G | |
ENST00000290650.8:c.1539+3A>G | ENSP00000290650.4:n.1539+3A>G | |
ENST00000546274.6:c.1539+3A>G | ENSP00000477932.1:n.1539+3A>G | |
ENST00000563239.1:c.*203-1100A>G | ENSP00000456502.1:n.*203-1100A>G | |
ENST00000569971.5:c.410+3A>G | ENSP00000455759.1:n.410+3A>G | |
NM_174916.2:c.1539+3A>G | NP_777576.1:n.1539+3A>G | |
NM_174916.3:c.1539+3A>G MANE Select | NP_777576.1:n.1539+3A>G |