HGVS | Genome Assembly |
---|---|
NC_000008.11:g.18400269T>C , CM000670.2:g.18400269T>C | GRCh38 |
NC_000008.10:g.18257779T>C , CM000670.1:g.18257779T>C | GRCh37 |
NC_000008.9:g.18302059T>C | NCBI36 |
NG_012246.1:g.14025T>C |
HGVS | Amino-acid change | |
---|---|---|
ENST00000286479.4:c.266T>C MANE Select | ENSP00000286479.3:p.Leu89Ser | |
ENST00000286479.3:c.266T>C | ENSP00000286479.3:p.Leu89Ser | |
ENST00000520116.1:c.-57-68T>C | ENSP00000428416.1:n.-57-68T>C | |
NM_000015.2:c.266T>C | NP_000006.2:p.Leu89Ser | |
XM_011544358.1:c.266T>C | XP_011542660.1:p.Leu89Ser | |
XM_017012938.1:c.266T>C | XP_016868427.1:p.Leu89Ser | |
NM_000015.3:c.266T>C MANE Select | NP_000006.2:p.Leu89Ser |