HGVS | Genome Assembly |
---|---|
NC_000008.11:g.63072993G>C , CM000670.2:g.63072993G>C | GRCh38 |
NC_000008.10:g.63985552G>C , CM000670.1:g.63985552G>C | GRCh37 |
NC_000008.9:g.64148106G>C | NCBI36 |
NG_016123.1:g.18061C>G |
HGVS | Amino-acid change | |
---|---|---|
ENST00000260116.5:c.300C>G MANE Select | ENSP00000260116.4:p.Tyr100Ter | |
ENST00000260116.4:c.300C>G | ENSP00000260116.4:p.Tyr100Ter | |
ENST00000521138.1:n.232+12825C>G | ||
NM_000370.3:c.300C>G MANE Select | NP_000361.1:p.Tyr100Ter | |
XM_006716468.2:c.205-8677C>G | XP_006716531.1:n.205-8677C>G | |
XM_006716468.4:c.205-8677C>G | XP_006716531.1:n.205-8677C>G |