HGVS | Genome Assembly |
---|---|
NC_000006.12:g.31547563T>G , CM000668.2:g.31547563T>G | GRCh38 |
NC_000006.11:g.31515340T>G , CM000668.1:g.31515340T>G | GRCh37 |
NC_000006.10:g.31623319T>G | NCBI36 |
NG_012344.1:g.5713T>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000376146.8:c.-13+590T>G (NFKBIL1) | ENSP00000365316.4:n.-13+590T>G | |
ENST00000415099.2:c.202+663A>C (ATP6V1G2) | ENSP00000390148.2:n.202+663A>C | |
NM_001144962.1:c.-13+590T>G (NFKBIL1) | NP_001138434.1:n.-13+590T>G | |
NM_001144963.1:c.-13+590T>G (NFKBIL1) | NP_001138435.1:n.-13+590T>G | |
NM_001144962.2:c.-13+590T>G (NFKBIL1) | NP_001138434.1:n.-13+590T>G | |
NM_001144963.2:c.-13+590T>G (NFKBIL1) | NP_001138435.1:n.-13+590T>G |