HGVS | Genome Assembly |
---|---|
NC_000001.11:g.196996133A>T , CM000663.2:g.196996133A>T | GRCh38 |
NC_000001.10:g.196965263A>T , CM000663.1:g.196965263A>T | GRCh37 |
NC_000001.9:g.195231886A>T | NCBI36 |
NG_016365.1:g.23597A>T , LRG_227:g.23597A>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000699466.1:c.647A>T | ENSP00000514393.1:p.Tyr216Phe | |
ENST00000699467.1:n.971A>T | ||
ENST00000699468.1:c.-5A>T | ENSP00000514394.1:n.-5A>T | |
ENST00000256785.5:c.902A>T MANE Select | ENSP00000256785.4:p.Tyr301Phe | |
ENST00000256785.4:c.902A>T | ENSP00000256785.4:p.Tyr301Phe | |
NM_030787.3:c.902A>T , LRG_227t1:c.902A>T | NP_110414.1:p.Tyr301Phe | |
XM_011510020.1:c.911A>T | XP_011508322.1:p.Tyr304Phe | |
XM_011510020.2:c.911A>T | XP_011508322.1:p.Tyr304Phe | |
NM_030787.4:c.902A>T MANE Select | NP_110414.1:p.Tyr301Phe |