HGVS | Genome Assembly |
---|---|
NC_000023.11:g.37805011C>G , CM000685.2:g.37805011C>G | GRCh38 |
NC_000023.10:g.37664264C>G , CM000685.1:g.37664264C>G | GRCh37 |
NC_000023.9:g.37549208C>G | NCBI36 |
NG_009065.1:g.29995C>G , LRG_53:g.29995C>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000696170.1:c.*666C>G | ENSP00000512461.1:n.*666C>G | |
ENST00000696171.1:c.1061C>G | ENSP00000512462.1:p.Ala354Gly | |
ENST00000378588.5:c.1157C>G MANE Select | ENSP00000367851.4:p.Ala386Gly | |
ENST00000378588.4:c.1157C>G | ENSP00000367851.4:p.Ala386Gly | |
ENST00000465127.1:c.171+379011C>G | ENSP00000417050.1:n.171+379011C>G | |
NM_000397.3:c.1157C>G , LRG_53t1:c.1157C>G | NP_000388.2:p.Ala386Gly | |
XM_011543890.1:c.851C>G | XP_011542192.1:p.Ala284Gly | |
NM_000397.4:c.1157C>G MANE Select | NP_000388.2:p.Ala386Gly |