HGVS | Genome Assembly |
---|---|
NC_000006.12:g.143485116T>G , CM000668.2:g.143485116T>G | GRCh38 |
NC_000006.11:g.143806253T>G , CM000668.1:g.143806253T>G | GRCh37 |
NC_000006.10:g.143847946T>G | NCBI36 |
NG_008459.1:g.39336T>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000367591.5:c.942-36T>G MANE Select | ENSP00000356563.4:n.942-36T>G | |
ENST00000367591.4:c.942-36T>G | ENSP00000356563.4:n.942-36T>G | |
ENST00000585848.1:n.45T>G | ||
NM_003630.2:c.942-36T>G | NP_003621.1:n.942-36T>G | |
NM_003630.3:c.942-36T>G MANE Select | NP_003621.1:n.942-36T>G |