HGVS | Genome Assembly |
---|---|
NC_000005.10:g.151259849T>G , CM000667.2:g.151259849T>G | GRCh38 |
NC_000005.9:g.150639410T>G , CM000667.1:g.150639410T>G | GRCh37 |
NC_000005.8:g.150619603T>G | NCBI36 |
NG_009059.1:g.11798T>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000357164.4:c.176T>G MANE Select | ENSP00000349687.3:p.Ile59Ser | |
ENST00000357164.3:c.176T>G | ENSP00000349687.3:p.Ile59Ser | |
ENST00000523004.1:c.51T>G | ||
ENST00000523466.5:c.221T>G | ENSP00000429100.1:p.Ile74Ser | |
NM_000405.4:c.176T>G | NP_000396.2:p.Ile59Ser | |
NM_001167607.1:c.176T>G | NP_001161079.1:p.Ile59Ser | |
NM_000405.5:c.176T>G MANE Select | NP_000396.2:p.Ile59Ser | |
NM_001167607.2:c.176T>G | NP_001161079.1:p.Ile59Ser | |
NM_001167607.3:c.176T>G | NP_001161079.1:p.Ile59Ser |