HGVS | Genome Assembly |
---|---|
NC_000020.11:g.33408816T>G , CM000682.2:g.33408816T>G | GRCh38 |
NC_000020.10:g.31996622T>G , CM000682.1:g.31996622T>G | GRCh37 |
NC_000020.9:g.31460283T>G | NCBI36 |
NG_011622.1:g.40077A>C , LRG_332:g.40077A>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000217381.3:c.1310A>C MANE Select | ENSP00000217381.2:p.Glu437Ala | |
ENST00000217381.2:c.1310A>C | ENSP00000217381.2:p.Glu437Ala | |
NM_003098.2:c.1310A>C , LRG_332t1:c.1310A>C | NP_003089.1:p.Glu437Ala | |
XM_005260517.1:c.1310A>C | XP_005260574.1:p.Glu437Ala | |
XM_011529007.1:c.1342A>C | XP_011527309.1:p.Ser448Arg | |
XM_011529008.1:c.1342A>C | XP_011527310.1:p.Ser448Arg | |
XR_936612.1:n.1346A>C | ||
XM_024451971.1:c.983A>C | XP_024307739.1:p.Glu328Ala | |
NM_003098.3:c.1310A>C MANE Select | NP_003089.1:p.Glu437Ala |