HGVS | Genome Assembly |
---|---|
NC_000010.11:g.94981216G>C , CM000672.2:g.94981216G>C | GRCh38 |
NC_000010.10:g.96740973G>C , CM000672.1:g.96740973G>C | GRCh37 |
NC_000010.9:g.96730963G>C | NCBI36 |
NG_008385.1:g.47559G>C | |
NG_008385.2:g.48059G>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000260682.8:c.995G>C MANE Select | ENSP00000260682.6:p.Gly332Ala | |
ENST00000643112.1:c.*4G>C | ENSP00000496202.1:n.*4G>C | |
ENST00000260682.6:c.995G>C | ENSP00000260682.6:p.Gly332Ala | |
NM_000771.3:c.995G>C | NP_000762.2:p.Gly332Ala | |
NM_000771.4:c.995G>C MANE Select | NP_000762.2:p.Gly332Ala |