HGVS | Genome Assembly |
---|---|
NC_000015.10:g.39581155A>G , CM000677.2:g.39581155A>G | GRCh38 |
NC_000015.9:g.39873356A>G , CM000677.1:g.39873356A>G | GRCh37 |
NC_000015.8:g.37660648A>G | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000260356.6:c.-103A>G MANE Select | ENSP00000260356.5:n.-103A>G | |
ENST00000260356.5:c.-103A>G | ENSP00000260356.5:n.-103A>G | |
ENST00000397591.2:c.-224A>G | ENSP00000380720.2:n.-224A>G | |
NM_003246.2:c.-103A>G | NP_003237.2:n.-103A>G | |
NM_003246.3:c.-103A>G | NP_003237.2:n.-103A>G | |
XM_011521970.1:c.-224A>G | XP_011520272.1:n.-224A>G | |
XM_011521971.1:c.-103A>G | XP_011520273.1:n.-103A>G | |
XR_931897.1:n.73A>G | ||
XM_011521971.2:c.-103A>G | XP_011520273.1:n.-103A>G | |
NM_003246.4:c.-103A>G MANE Select | NP_003237.2:n.-103A>G |