HGVS | Genome Assembly |
---|---|
NC_000018.10:g.31326548A>G , CM000680.2:g.31326548A>G | GRCh38 |
NC_000018.9:g.28906511A>G , CM000680.1:g.28906511A>G | GRCh37 |
NC_000018.8:g.27160509A>G | NCBI36 |
NG_011803.2:g.13460A>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000257192.5:c.49-33A>G MANE Select | ENSP00000257192.4:n.49-33A>G | |
ENST00000257192.4:c.49-33A>G | ENSP00000257192.4:n.49-33A>G | |
NM_001942.3:c.49-33A>G | NP_001933.2:n.49-33A>G | |
NM_001942.4:c.49-33A>G MANE Select | NP_001933.2:n.49-33A>G |