HGVS | Genome Assembly |
---|---|
NC_000012.12:g.111803871T>G , CM000674.2:g.111803871T>G | GRCh38 |
NC_000012.11:g.112241675T>G , CM000674.1:g.112241675T>G | GRCh37 |
NC_000012.10:g.110726058T>G | NCBI36 |
NG_012250.1:g.42330T>G | |
NG_012250.2:g.41985T>G |
HGVS | Amino-acid change | |
---|---|---|
ENST00000261733.7:c.1419T>G MANE Select | ENSP00000261733.2:p.Tyr473Ter | |
ENST00000261733.6:c.1419T>G | ENSP00000261733.2:p.Tyr473Ter | |
ENST00000416293.7:c.1278T>G | ENSP00000403349.3:p.Tyr426Ter | |
ENST00000548536.1:c.*1295T>G | ENSP00000448179.1:n.*1295T>G | |
ENST00000549106.1:c.350T>G | ||
NM_000690.3:c.1419T>G | NP_000681.2:p.Tyr473Ter | |
NM_001204889.1:c.1278T>G | NP_001191818.1:p.Tyr426Ter | |
NM_000690.4:c.1419T>G MANE Select | NP_000681.2:p.Tyr473Ter | |
NM_001204889.2:c.1278T>G | NP_001191818.1:p.Tyr426Ter |