HGVS | Genome Assembly |
---|---|
NC_000008.11:g.18400311C>G , CM000670.2:g.18400311C>G | GRCh38 |
NC_000008.10:g.18257821C>G , CM000670.1:g.18257821C>G | GRCh37 |
NC_000008.9:g.18302101C>G | NCBI36 |
NG_012246.1:g.14067C>G |
HGVS | Amino-acid change | |
---|---|---|
ENST00000286479.4:c.308C>G MANE Select | ENSP00000286479.3:p.Thr103Ser | |
ENST00000286479.3:c.308C>G | ENSP00000286479.3:p.Thr103Ser | |
ENST00000520116.1:c.-57-26C>G | ENSP00000428416.1:n.-57-26C>G | |
NM_000015.2:c.308C>G | NP_000006.2:p.Thr103Ser | |
XM_011544358.1:c.308C>G | XP_011542660.1:p.Thr103Ser | |
XM_017012938.1:c.308C>G | XP_016868427.1:p.Thr103Ser | |
NM_000015.3:c.308C>G MANE Select | NP_000006.2:p.Thr103Ser |