HGVS | Genome Assembly |
---|---|
NC_000005.10:g.146340085G>C , CM000667.2:g.146340085G>C | GRCh38 |
NC_000005.9:g.145719648G>C , CM000667.1:g.145719648G>C | GRCh37 |
NC_000005.8:g.145699841G>C | NCBI36 |
NG_011885.1:g.6062G>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000646991.2:c.658G>C MANE Select | ENSP00000495718.1:p.Val220Leu | |
ENST00000230732.4:c.658G>C | ENSP00000230732.4:p.Val220Leu | |
NM_002700.2:c.658G>C | NP_002691.1:p.Val220Leu | |
NM_002700.3:c.658G>C MANE Select | NP_002691.1:p.Val220Leu |