HGVS | Genome Assembly |
---|---|
NC_000020.11:g.33716858G>A , CM000682.2:g.33716858G>A | GRCh38 |
NC_000020.10:g.32304664G>A , CM000682.1:g.32304664G>A | GRCh37 |
NC_000020.9:g.31768325G>A | NCBI36 |
HGVS | Amino-acid change | |
---|---|---|
ENST00000409299.8:c.114-2122C>T MANE Select | ENSP00000386385.3:n.114-2122C>T | |
ENST00000217398.3:c.114-2122C>T | ENSP00000217398.3:n.114-2122C>T | |
ENST00000344022.7:c.114-2122C>T | ENSP00000343071.3:n.114-2122C>T | |
ENST00000409299.7:c.114-2122C>T | ENSP00000386385.3:n.114-2122C>T | |
NM_007238.4:c.114-2122C>T | NP_009169.3:n.114-2122C>T | |
NM_183397.2:c.114-2122C>T | NP_899634.1:n.114-2122C>T | |
NM_007238.5:c.114-2122C>T MANE Select | NP_009169.3:n.114-2122C>T | |
NM_183397.3:c.114-2122C>T | NP_899634.1:n.114-2122C>T |