HGVS | Genome Assembly |
---|---|
NC_000015.10:g.48474268G>C , CM000677.2:g.48474268G>C | GRCh38 |
NC_000015.9:g.48766465G>C , CM000677.1:g.48766465G>C | GRCh37 |
NC_000015.8:g.46553757G>C | NCBI36 |
NG_008805.2:g.176521C>G , LRG_778:g.176521C>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000559133.6:c.4197C>G | ENSP00000453958.2:p.Gly1399= | |
ENST00000674301.2:c.4197C>G | ENSP00000501333.2:p.Gly1399= | |
ENST00000684448.1:n.2871C>G | ||
ENST00000316623.10:c.4197C>G MANE Select | ENSP00000325527.5:p.Gly1399= | |
ENST00000316623.9:c.4197C>G | ENSP00000325527.5:p.Gly1399= | |
ENST00000537463.6:c.869C>G | ENSP00000440294.2:p.Ala290Gly | |
NM_000138.4:c.4197C>G , LRG_778t1:c.4197C>G | NP_000129.3:p.Gly1399= | |
NM_000138.5:c.4197C>G MANE Select | NP_000129.3:p.Gly1399= |