HGVS | Genome Assembly |
---|---|
NC_000020.11:g.64049240T>A , CM000682.2:g.64049240T>A | GRCh38 |
NC_000020.10:g.62680593T>A , CM000682.1:g.62680593T>A | GRCh37 |
NC_000020.9:g.62151037T>A | NCBI36 |
NG_008095.1:g.5387A>T |
HGVS | Amino-acid change | |
---|---|---|
ENST00000340356.9:c.277A>T (SOX18) MANE Select | ENSP00000341815.7:p.Met93Leu | |
ENST00000340356.8:c.277A>T (SOX18) | ENSP00000341815.7:p.Met93Leu | |
NM_018419.2:c.277A>T (SOX18) | NP_060889.1:p.Met93Leu | |
XM_011529022.1:c.-2320+6845T>A (TCEA2) | XP_011527324.1:n.-2320+6845T>A | |
XM_011529025.1:c.-2236+6845T>A (TCEA2) | XP_011527327.1:n.-2236+6845T>A | |
XM_024451978.1:c.-2236+6845T>A (TCEA2) | XP_024307746.1:n.-2236+6845T>A | |
NM_018419.3:c.277A>T (SOX18) MANE Select | NP_060889.1:p.Met93Leu |