HGVS | Genome Assembly |
---|---|
NC_000002.12:g.218812735C>G , CM000664.2:g.218812735C>G | GRCh38 |
NC_000002.11:g.219677458C>G , CM000664.1:g.219677458C>G | GRCh37 |
NC_000002.10:g.219385702C>G | NCBI36 |
NG_007959.1:g.35987C>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000258415.9:c.830C>G MANE Select | ENSP00000258415.4:p.Ala277Gly | |
ENST00000258415.8:c.830C>G | ENSP00000258415.4:p.Ala277Gly | |
ENST00000411688.1:c.548C>G | ENSP00000392671.1:p.Ala183Gly | |
ENST00000445971.1:c.*291C>G | ENSP00000404945.1:n.*291C>G | |
ENST00000466602.1:n.778C>G | ||
ENST00000494263.5:n.1264C>G | ||
NM_000784.3:c.830C>G | NP_000775.1:p.Ala277Gly | |
XM_017003488.2:c.410C>G | XP_016858977.1:p.Ala137Gly | |
NM_000784.4:c.830C>G MANE Select | NP_000775.1:p.Ala277Gly |