HGVS | Genome Assembly |
---|---|
NC_000023.11:g.37805084G>T , CM000685.2:g.37805084G>T | GRCh38 |
NC_000023.10:g.37664337G>T , CM000685.1:g.37664337G>T | GRCh37 |
NC_000023.9:g.37549281G>T | NCBI36 |
NG_009065.1:g.30068G>T , LRG_53:g.30068G>T |
HGVS | Amino-acid change | |
---|---|---|
ENST00000696170.1:c.*739G>T | ENSP00000512461.1:n.*739G>T | |
ENST00000696171.1:c.1134G>T | ENSP00000512462.1:p.Gly378= | |
ENST00000378588.5:c.1230G>T MANE Select | ENSP00000367851.4:p.Gly410= | |
ENST00000378588.4:c.1230G>T | ENSP00000367851.4:p.Gly410= | |
ENST00000465127.1:c.171+379084G>T | ENSP00000417050.1:n.171+379084G>T | |
NM_000397.3:c.1230G>T , LRG_53t1:c.1230G>T | NP_000388.2:p.Gly410= | |
XM_011543890.1:c.924G>T | XP_011542192.1:p.Gly308= | |
NM_000397.4:c.1230G>T MANE Select | NP_000388.2:p.Gly410= |