HGVS | Genome Assembly |
---|---|
NC_000019.10:g.6714027A>T , CM000681.2:g.6714027A>T | GRCh38 |
NC_000019.9:g.6714038A>T , CM000681.1:g.6714038A>T | GRCh37 |
NC_000019.8:g.6665038A>T | NCBI36 |
NG_009557.1:g.11625T>A , LRG_27:g.11625T>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000695652.1:c.615T>A | ENSP00000512083.1:p.Tyr205Ter | |
ENST00000245907.11:c.738T>A MANE Select | ENSP00000245907.4:p.Tyr246Ter | |
ENST00000245907.10:c.738T>A | ENSP00000245907.4:p.Tyr246Ter | |
ENST00000595577.1:n.242T>A | ||
NM_000064.3:c.738T>A | NP_000055.2:p.Tyr246Ter | |
NM_000064.4:c.738T>A MANE Select | NP_000055.2:p.Tyr246Ter |