HGVS | Genome Assembly |
---|---|
NC_000023.11:g.64192424T>G , CM000685.2:g.64192424T>G | GRCh38 |
NC_000023.10:g.63412304T>G , CM000685.1:g.63412304T>G | GRCh37 |
NC_000023.9:g.63329029T>G | NCBI36 |
NG_021345.1:g.18321A>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000374869.8:c.863A>C MANE Select | ENSP00000364003.4:p.Glu288Ala | |
ENST00000330258.3:c.863A>C | ENSP00000329117.3:p.Glu288Ala | |
ENST00000374869.7:c.863A>C | ENSP00000364003.3:p.Glu288Ala | |
NM_152424.3:c.863A>C | NP_689637.3:p.Glu288Ala | |
XM_011530858.1:c.863A>C | XP_011529160.1:p.Glu288Ala | |
NM_152424.4:c.863A>C MANE Select | NP_689637.3:p.Glu288Ala |