HGVS | Genome Assembly |
---|---|
NC_000004.12:g.52028799A>T , CM000666.2:g.52028799A>T | GRCh38 |
NC_000004.11:g.52894965A>T , CM000666.1:g.52894965A>T | GRCh37 |
NC_000004.10:g.52589722A>T | NCBI36 |
NG_008891.1:g.14521T>A , LRG_204:g.14521T>A |
HGVS | Amino-acid change | |
---|---|---|
ENST00000381431.10:c.552T>A MANE Select | ENSP00000370839.6:p.Tyr184Ter | |
ENST00000381431.9:c.552T>A | ENSP00000370839.5:p.Tyr184Ter | |
ENST00000506357.5:c.635T>A | ||
NM_000232.4:c.552T>A , LRG_204t1:c.552T>A | NP_000223.1:p.Tyr184Ter | |
XM_006714049.2:c.255T>A | XP_006714112.1:p.Tyr85Ter | |
XM_011534403.1:c.342T>A | XP_011532705.1:p.Tyr114Ter | |
XM_011534404.1:c.255T>A | XP_011532706.1:p.Tyr85Ter | |
NM_000232.5:c.552T>A MANE Select | NP_000223.1:p.Tyr184Ter |