HGVS | Genome Assembly |
---|---|
NC_000016.10:g.28845037C>G , CM000678.2:g.28845037C>G | GRCh38 |
NC_000016.9:g.28856358C>G , CM000678.1:g.28856358C>G | GRCh37 |
NC_000016.8:g.28763859C>G | NCBI36 |
NG_008964.1:g.6372G>C | |
NG_029706.2:g.3438C>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000313511.8:c.433G>C MANE Select | ENSP00000322439.3:p.Ala145Pro | |
ENST00000313511.7:c.433G>C | ENSP00000322439.3:p.Ala145Pro | |
ENST00000565012.1:c.266G>C | ENSP00000455007.1:p.Cys89Ser | |
NM_003321.4:c.433G>C | NP_003312.3:p.Ala145Pro | |
XM_011545928.1:c.433G>C | XP_011544230.1:p.Ala145Pro | |
NM_001365360.1:c.433G>C | NP_001352289.1:p.Ala145Pro | |
NM_003321.5:c.433G>C MANE Select | NP_003312.3:p.Ala145Pro | |
NM_001365360.2:c.433G>C | NP_001352289.1:p.Ala145Pro |