HGVS | Genome Assembly |
---|---|
NC_000023.11:g.154966665T= , CM000685.2:g.154966665T= | GRCh38 |
NC_000023.10:g.154194940T= , CM000685.1:g.154194940T= | GRCh37 |
NC_000023.9:g.153848134T= | NCBI36 |
NG_011403.1:g.61059A= | |
NG_011403.2:g.61059A= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000360256.9:c.1032A= MANE Select | ENSP00000353393.4:p.Lys344= | |
ENST00000647125.1:c.*908A= | ENSP00000496062.1:n.*908A= | |
ENST00000360256.8:c.1032A= | ENSP00000353393.4:p.Lys344= | |
NM_000132.3:c.1032A= | NP_000123.1:p.Lys344= | |
XM_011531126.1:c.927A= | XP_011529428.1:p.Lys309= | |
NM_000132.4:c.1032A= MANE Select | NP_000123.1:p.Lys344= |