HGVS | Genome Assembly |
---|---|
NC_000007.14:g.17339841T>A , CM000669.2:g.17339841T>A | GRCh38 |
NC_000007.13:g.17379465T>A , CM000669.1:g.17379465T>A | GRCh37 |
NC_000007.12:g.17345990T>A | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000242057.9:c.2016T>A MANE Select | ENSP00000242057.4:p.Tyr672Ter | |
ENST00000637807.1:c.1986T>A | ENSP00000490530.1:p.Tyr662Ter | |
ENST00000642825.1:c.1971T>A | ENSP00000495987.1:p.Tyr657Ter | |
ENST00000242057.8:c.2016T>A | ENSP00000242057.4:p.Tyr672Ter | |
ENST00000463496.1:c.2016T>A | ENSP00000436466.1:p.Tyr672Ter | |
NM_001621.4:c.2016T>A | NP_001612.1:p.Tyr672Ter | |
NM_001621.5:c.2016T>A MANE Select | NP_001612.1:p.Tyr672Ter |