HGVS | Genome Assembly |
---|---|
NC_000010.11:g.133532177G>A , CM000672.2:g.133532177G>A | GRCh38 |
NC_000010.10:g.135345681G>A , CM000672.1:g.135345681G>A | GRCh37 |
NC_000010.9:g.135195671G>A | NCBI36 |
NG_008383.1:g.9815G>A |
HGVS | Amino-acid change | |
---|---|---|
ENST00000252945.8:c.541G>A MANE Select | ENSP00000252945.3:p.Ala181Thr | |
ENST00000252945.7:c.541G>A | ENSP00000252945.3:p.Ala181Thr | |
ENST00000368520.1:n.602G>A | ||
ENST00000418356.1:c.130G>A | ENSP00000397299.1:p.Ala44Thr | |
ENST00000421586.5:c.280G>A | ENSP00000412754.1:p.Ala94Thr | |
ENST00000463117.6:c.541G>A | ENSP00000440689.1:p.Ala181Thr | |
ENST00000477500.5:n.448+443G>A | ||
ENST00000541080.5:c.226+443G>A | ||
NM_000773.3:c.541G>A | NP_000764.1:p.Ala181Thr | |
NM_000773.4:c.541G>A MANE Select | NP_000764.1:p.Ala181Thr |