HGVS | Genome Assembly |
---|---|
NC_000020.11:g.64049244G>C , CM000682.2:g.64049244G>C | GRCh38 |
NC_000020.10:g.62680597G>C , CM000682.1:g.62680597G>C | GRCh37 |
NC_000020.9:g.62151041G>C | NCBI36 |
NG_008095.1:g.5383C>G |
HGVS | Amino-acid change | |
---|---|---|
ENST00000340356.9:c.273C>G (SOX18) MANE Select | ENSP00000341815.7:p.Ala91= | |
ENST00000340356.8:c.273C>G (SOX18) | ENSP00000341815.7:p.Ala91= | |
NM_018419.2:c.273C>G (SOX18) | NP_060889.1:p.Ala91= | |
XM_011529022.1:c.-2320+6849G>C (TCEA2) | XP_011527324.1:n.-2320+6849G>C | |
XM_011529025.1:c.-2236+6849G>C (TCEA2) | XP_011527327.1:n.-2236+6849G>C | |
XM_024451978.1:c.-2236+6849G>C (TCEA2) | XP_024307746.1:n.-2236+6849G>C | |
NM_018419.3:c.273C>G (SOX18) MANE Select | NP_060889.1:p.Ala91= |