HGVS | Genome Assembly |
---|---|
NC_000011.10:g.47338555C>G , CM000673.2:g.47338555C>G | GRCh38 |
NC_000011.9:g.47360106C>G , CM000673.1:g.47360106C>G | GRCh37 |
NC_000011.8:g.47316682C>G | NCBI36 |
NG_007667.1:g.19148G>C , LRG_386:g.19148G>C |
HGVS | Amino-acid change | |
---|---|---|
ENST00000545968.6:c.2273G>C MANE Select | ENSP00000442795.1:p.Gly758Ala | |
ENST00000256993.8:c.2273G>C | ENSP00000256993.5:p.Gly758Ala | |
ENST00000399249.6:c.2273G>C | ENSP00000382193.2:p.Gly758Ala | |
ENST00000544791.1:c.2273G>C | ENSP00000444259.1:p.Gly758Ala | |
ENST00000545968.5:c.2273G>C | ENSP00000442795.1:p.Gly758Ala | |
NM_000256.3:c.2273G>C , LRG_386t1:c.2273G>C MANE Select | NP_000247.2:p.Gly758Ala | |
XM_011520117.1:c.2255G>C | XP_011518419.1:p.Gly752Ala | |
XM_011520118.1:c.2192G>C | XP_011518420.1:p.Gly731Ala |