HGVS | Genome Assembly |
---|---|
NC_000007.14:g.45913536A>G , CM000669.2:g.45913536A>G | GRCh38 |
NC_000007.13:g.45953135A>G , CM000669.1:g.45953135A>G | GRCh37 |
NC_000007.12:g.45919660A>G | NCBI36 |
NG_011508.1:g.12737T>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000613132.5:c.*314T>C MANE Select | ENSP00000477772.2:n.*314T>C | |
ENST00000381083.9:c.*314T>C | ENSP00000370473.4:n.*314T>C | |
ENST00000275521.10:c.*314T>C | ENSP00000275521.5:n.*314T>C | |
ENST00000381086.9:c.*314T>C | ENSP00000370476.4:n.*314T>C | |
ENST00000613132.4:c.1127T>C | ENSP00000477772.1:n.1127T>C | |
NM_000598.4:c.*314T>C | NP_000589.2:n.*314T>C | |
NM_001013398.1:c.*314T>C | NP_001013416.1:n.*314T>C | |
NM_001013398.2:c.*314T>C | NP_001013416.1:n.*314T>C | |
NM_000598.5:c.*314T>C MANE Select | NP_000589.2:n.*314T>C |