HGVS | Genome Assembly |
---|---|
NC_000023.11:g.25013709G>C , CM000685.2:g.25013709G>C | GRCh38 |
NC_000023.10:g.25031826G>C , CM000685.1:g.25031826G>C | GRCh37 |
NC_000023.9:g.24941747G>C | NCBI36 |
NG_008281.1:g.7240C>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000379044.5:c.286C>G MANE Select | ENSP00000368332.4:p.Leu96Val | |
ENST00000379044.4:c.286C>G | ENSP00000368332.4:p.Leu96Val | |
NM_139058.2:c.286C>G | NP_620689.1:p.Leu96Val | |
NM_139058.3:c.286C>G MANE Select | NP_620689.1:p.Leu96Val |