HGVS | Genome Assembly |
---|---|
NC_000016.10:g.30737191A>T , CM000678.2:g.30737191A>T | GRCh38 |
NC_000016.9:g.30748512A>T , CM000678.1:g.30748512A>T | GRCh37 |
NC_000016.8:g.30656013A>T | NCBI36 |
NG_032135.1:g.43051A>T |
HGVS | Amino-acid change | |
---|---|---|
ENST00000411466.7:c.7151A>T | ENSP00000405186.3:p.Lys2384Met | |
ENST00000704023.1:c.1431A>T | ||
ENST00000706321.1:c.7151A>T | ENSP00000516346.1:p.Lys2384Met | |
ENST00000262518.9:c.7151A>T MANE Select | ENSP00000262518.4:p.Lys2384Met | |
ENST00000262518.8:c.7151A>T | ENSP00000262518.4:p.Lys2384Met | |
ENST00000380361.7:c.6620A>T | ENSP00000369719.3:p.Lys2207Met | |
ENST00000395059.6:c.6374A>T | ENSP00000378499.3:p.Lys2125Met | |
NM_006662.2:c.7151A>T | NP_006653.2:p.Lys2384Met | |
NM_006662.3:c.7151A>T MANE Select | NP_006653.2:p.Lys2384Met |