HGVS | Genome Assembly |
---|---|
NC_000001.11:g.150989393A>G , CM000663.2:g.150989393A>G | GRCh38 |
NC_000001.10:g.150961869A>G , CM000663.1:g.150961869A>G | GRCh37 |
NC_000001.9:g.149228493A>G | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000368947.9:c.852+1052A>G MANE Select | ENSP00000357943.4:n.852+1052A>G | |
ENST00000368947.8:c.852+1052A>G | ENSP00000357943.4:n.852+1052A>G | |
NM_003568.2:c.852+1052A>G | NP_003559.2:n.852+1052A>G | |
XM_005245539.3:c.852+1052A>G | XP_005245596.1:n.852+1052A>G | |
XM_011510058.1:c.852+1052A>G | XP_011508360.1:n.852+1052A>G | |
XM_011510058.3:c.852+1052A>G | XP_011508360.1:n.852+1052A>G | |
NM_003568.3:c.852+1052A>G MANE Select | NP_003559.2:n.852+1052A>G |