HGVS | Genome Assembly |
---|---|
NC_000001.11:g.94007545C>A , CM000663.2:g.94007545C>A | GRCh38 |
NC_000001.10:g.94473101C>A , CM000663.1:g.94473101C>A | GRCh37 |
NC_000001.9:g.94245689C>A | NCBI36 |
NG_009073.1:g.118605G>T |
HGVS | Amino-acid change | |
---|---|---|
ENST00000370225.4:c.6005+89G>T MANE Select | ENSP00000359245.3:n.6005+89G>T | |
ENST00000370225.3:c.6005+89G>T | ENSP00000359245.3:n.6005+89G>T | |
ENST00000465352.1:n.421+89G>T | ||
ENST00000484388.1:n.119+89G>T | ||
ENST00000536513.5:c.2381+89G>T | ENSP00000439707.2:n.2381+89G>T | |
NM_000350.2:c.6005+89G>T | NP_000341.2:n.6005+89G>T | |
NM_000350.3:c.6005+89G>T MANE Select | NP_000341.2:n.6005+89G>T |