HGVS | Genome Assembly |
---|---|
NC_000023.11:g.37803981G= , CM000685.2:g.37803981G= | GRCh38 |
NC_000023.10:g.37663234G= , CM000685.1:g.37663234G= | GRCh37 |
NC_000023.9:g.37548178G= | NCBI36 |
NG_009065.1:g.28965G= , LRG_53:g.28965G= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000696170.1:c.*511G= | ENSP00000512461.1:n.*511G= | |
ENST00000696171.1:c.906G= | ENSP00000512462.1:p.Lys302= | |
ENST00000378588.5:c.1002G= MANE Select | ENSP00000367851.4:p.Lys334= | |
ENST00000378588.4:c.1002G= | ENSP00000367851.4:p.Lys334= | |
ENST00000465127.1:c.171+377981G= | ENSP00000417050.1:n.171+377981G= | |
ENST00000492288.1:n.427G= | ||
NM_000397.3:c.1002G= , LRG_53t1:c.1002G= | NP_000388.2:p.Lys334= | |
XM_011543890.1:c.696G= | XP_011542192.1:p.Lys232= | |
NM_000397.4:c.1002G= MANE Select | NP_000388.2:p.Lys334= |