HGVS | Genome Assembly |
---|---|
NC_000023.11:g.154997038T= , CM000685.2:g.154997038T= | GRCh38 |
NC_000023.10:g.154225313T= , CM000685.1:g.154225313T= | GRCh37 |
NC_000023.9:g.153878507T= | NCBI36 |
NG_011403.1:g.30686A= | |
NG_011403.2:g.30686A= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000360256.9:c.323A= MANE Select | ENSP00000353393.4:p.Lys108= | |
ENST00000647125.1:c.*109A= | ENSP00000496062.1:n.*109A= | |
ENST00000360256.8:c.323A= | ENSP00000353393.4:p.Lys108= | |
ENST00000423959.5:c.218A= | ENSP00000409446.1:p.Lys73= | |
ENST00000453950.1:c.305A= | ENSP00000389153.1:p.Lys102= | |
NM_000132.3:c.323A= | NP_000123.1:p.Lys108= | |
XM_011531126.1:c.218A= | XP_011529428.1:p.Lys73= | |
NM_000132.4:c.323A= MANE Select | NP_000123.1:p.Lys108= |